Heat Shock 22 kDa Protein-Related Disorders via the HSPB8 Gene |
Sanger Sequencing |
$460 |
Sequencing with CNV PGxome |
$890 |
|
Heat Shock 27 kDa Protein-Related Disorders via the HSPB1 Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV PGxome |
$890 |
|
Helsmoortel-Van der Aa Syndrome via the ADNP Gene |
Sanger Sequencing |
$990 |
Sequencing with CNV PGxome |
$890 |
|
Hemiplegic Migraine and PRRT2-Related Disorders via the PRRT2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hemophilia A via the F8 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hemophilia B via the F9 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hemophilia C via the F11 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hennekam Lymphangiectasia-Lymphedema Syndrome via the CCBE1 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Angioedema via the SERPING1 /C1NH Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Breast and Ovarian Cancer via the BARD1 Gene |
Sequencing with CNV PG-Select |
$540 |
|
Hereditary Breast and Ovarian Cancer via the RAD50 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Breast and Ovarian Cancer via the RAD51D Gene |
Sequencing with CNV PG-Select |
$540 |
|
Hereditary Breast Cancer via the CHEK2 Gene |
Sequencing with CNV PG-Select |
$540 |
|
Hereditary Coproporphyria via the CPOX Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Diffuse Gastric Cancer via the CDH1 Gene |
Sequencing with CNV PG-Select |
$540 |
|
Hereditary Diffuse Leukoencephalopathy with Spheroids via the CSF1R Gene |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Folate Malabsorption via the SLC46A1 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Fructose Intolerance via the ALDOB Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Hemochromatosis via the HFE Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Hemochromatosis via the SLC40A1 Gene |
Sanger Sequencing |
$870 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Hemochromatosis via the TFR2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Hemorrhagic Telangiectasia Type 1 (HHT1) / Osler-Weber-Rendu Disease via the ENG Gene |
Sanger Sequencing |
$990 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Hemorrhagic Telangiectasia Type 2 (HHT2) via the ACVRL1/ALK1 Gene |
Sanger Sequencing |
$770 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Leiomyomatosis and Renal Cell Cancer or Fumarase Deficiency via the FH Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Lymphedema via the GJC2 Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Mixed Polyposis Syndrome via the GREM1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Motor and Sensory Neuropathy IIB (HMSN2B) via the RAB7A Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Multiple Osteochondromas (HMO) via the EXT1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Multiple Osteochondromas (HMO) via the EXT2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Myelodysplastic Syndrome (MDS) / Acute Myeloid Leukemia (AML) via the DDX41 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Neuroblastoma via the ALK Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Neuroblastoma via the KIF1B Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Neuroblastoma via the PHOX2B Gene |
Sequencing with CNV PG-Select |
$540 |
|
Hereditary Papillary Renal Cell Carcinoma via the MET Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the MAX Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHA Gene |
Sequencing with CNV PG-Select |
$540 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHAF2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHB Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHC Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHD Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome via the TMEM127 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hereditary Sensory and Autonomic Neuropathy Type V (HSAN5) via the NGF Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Sensory and Autonomic Neuropathy Type VIII via the PRDM12 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Sensory Neuropathy Type IA via the SPTLC1 Gene |
Sanger Sequencing |
$1130 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Sensory Neuropathy with Spastic Paraplegia via the CCT5 Gene |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Sensory Neuropathy, Type IE via the DNMT1 Gene |
Sanger Sequencing |
$1960 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spastic Paraplegia (HSP) via the ENTPD1 Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spastic Paraplegia via the ATP2B4 (PMCA4) Gene |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spherocytosis Type 1 via the ANK1 Gene |
Sanger Sequencing |
$1960 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spherocytosis via the EPB42 Gene |
Sanger Sequencing |
$870 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spherocytosis via the SLC4A1 Gene |
Sanger Sequencing |
$1190 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spherocytosis/Elliptocytosis via the SPTA1 Gene |
Sanger Sequencing |
$2550 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Spherocytosis/Elliptocytosis via the SPTB Gene |
Sanger Sequencing |
$1720 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Thrombocythemia via the THPO Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Hereditary Xerocytosis via the PIEZO1 Gene |
Sanger Sequencing |
$2520 |
Sequencing with CNV PGxome |
$890 |
|
Hermansky-Pudlak Syndrome Type 1 (HPS1) via the HPS1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hermansky-Pudlak Syndrome Type 2 (HPS2) via the AP3B1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hermansky-Pudlak Syndrome Type 3 (HPS3) via the HPS3 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hermansky-Pudlak Syndrome Type 4 (HPS4) via the HPS4 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hermansky-Pudlak Syndrome Type 5 (HPS5) via the HPS5 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hermansky-Pudlak Syndrome Type 6 (HPS6) via the HPS6 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hermansky-Pudlak Syndrome Type 7 (HPS7) via the DTNBP1 Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV PGxome |
$890 |
|
Hermansky-Pudlak Syndrome Type 8 (HPS8) via the BLOC1S3 Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV PGxome |
$890 |
|
Hermansky-Pudlak Syndrome Type 9 (HPS9) via the BLOC1S6/PLDN Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV PGxome |
$890 |
|
Hermansky-Pudlak Syndrome via the HPS3 Gene, Exon 1 Deletion |
|
HESX1-Related Disorders via the HESX1 Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Heterotaxy and Conotruncal Heart Defects via the GDF1 Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Heterotaxy via the LEFTY2 Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV PGxome |
$890 |
|
Heterotaxy, Visceral 4 (HTX4) via the ACVR2B Gene |
Sanger Sequencing |
$810 |
Sequencing with CNV PGxome |
$890 |
|
Heterotaxy, Visceral 5 (HTX5) via the NODAL Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Hirschsprung Disease (HSCR) via the RET Gene |
Sequencing with CNV PGxome |
$890 |
|
Hirschsprung Disease 2 (HSCR2) via the EDNRB Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Hirschsprung Disease 3 (HSCR3) via the GDNF Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV PGxome |
$890 |
|
Hirschsprung Disease 4 (HSCR4) via the EDN3 Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Hirschsprung Disease via the NRTN Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV PGxome |
$890 |
|
Hirschsprung Disease, Cardiac Defects and Autonomic Dysfunction via the ECE1 Gene |
Sanger Sequencing |
$1160 |
Sequencing with CNV PGxome |
$890 |
|
Histiocytosis-Lymphadenopathy Plus Syndrome via the SLC29A3 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV PGxome |
$890 |
|
Holocarboxylase Synthetase Deficiency via the HLCS Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV PGxome |
$890 |
|
Holoprosencephaly-11 via the CDON Gene |
Sanger Sequencing |
$1270 |
Sequencing with CNV PGxome |
$890 |
|
Holoprosencephaly-2 (Autosomal Dominant, Nonsyndromic) via the SIX3 Gene |
Sanger Sequencing |
$560 |
Sequencing with CNV PGxome |
$890 |
|
Holoprosencephaly-3 (Autosomal Dominant Nonsyndromic) via the SHH Gene |
Sanger Sequencing |
$670 |
Sequencing with CNV PGxome |
$890 |
|
Holoprosencephaly-4 (Autosomal Dominant, Nonsyndromic) via the TGIF1 Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV PGxome |
$890 |
|
Holoprosencephaly-5 (Autosomal Dominant, Nonsyndromic) via the ZIC2 Gene |
Sanger Sequencing |
$730 |
Sequencing with CNV PGxome |
$890 |
|
Holoprosencephaly-7 (Autosomal Dominant, Nonsyndromic) via the PTCH1 Gene |
Sequencing with CNV PG-Select |
$540 |
|
Holoprosencephaly-9 (Autosomal Dominant, Nonsyndromic) via the GLI2 Gene |
Sanger Sequencing |
$1080 |
Sequencing with CNV PGxome |
$890 |
|
Holt-Oram Syndrome (HOS) via the TBX5 Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV PGxome |
$890 |
|
Homocystinuria via the CBS Gene |
Sanger Sequencing |
$1100 |
Sequencing with CNV PGxome |
$890 |
|
Homocystinuria, cblE Type, via the MTRR Gene |
Sanger Sequencing |
$1060 |
Sequencing with CNV PGxome |
$890 |
|
Homocystinuria, cblG Type, via the MTR Gene |
Sanger Sequencing |
$1650 |
Sequencing with CNV PGxome |
$890 |
|
Huntington Disease via the HTT CAG Repeat Expansion |
Repeat-Primed PCR & Fragment Length |
$250 |
|
Hyaline Fibromatosis Syndrome via the ANTXR2 Gene |
Sanger Sequencing |
$1060 |
Sequencing with CNV PGxome |
$890 |
|
Hydrocephalus, Congenital 2 with or without Brain or Eye Anomalies via the MPDZ Gene |
Sequencing with CNV PGxome |
$890 |
|
Hydrocephalus, Congenital, 1 via the CCDC88C Gene |
Sequencing with CNV PGxome |
$890 |
|
Hydroxyprolinemia via the PRODH2 Gene |
Sanger Sequencing |
$810 |
Sequencing with CNV PGxome |
$890 |
|
Hyper IgD Syndrome/Mevalonate Aciduria via the MVK Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV PGxome |
$890 |
|
Hyper IgM Syndrome via the AICDA Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Hyperammonemia via the NAGS Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Hypercalcemic and Hypocalcemic Disorders via the CASR Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hypercalcemic and Hypocalcemic Disorders via the GNA11 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV PGxome |
$890 |
|
Hypercalciuria via the ADCY10 Gene |
Sanger Sequencing |
$1620 |
Sequencing with CNV PGxome |
$890 |
|
Hyperglycemia and Hypoglycemia via the GCK Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV PGxome |
$890 |
|
Hyperphenylalaninemia via the DNAJC12 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Hyperphosphatasia with Intellectual Disability via the PIGO Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hypertension and Brachydactyly Syndrome via the PDE3A Gene |
Sanger Sequencing |
$1190 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the ACTN2 Gene |
Sanger Sequencing |
$1060 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the CSRP3 Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the MYH6 Gene |
Sanger Sequencing |
$1560 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the PLN Gene |
Sanger Sequencing |
$370 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the TPM1 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the VCL Gene |
Sanger Sequencing |
$1130 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and other MYH7-Related Disorders via the MYH7 Gene |
Sanger Sequencing |
$1590 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Related Disorders via the ACTC1 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Related Disorders via the TNNI3 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy and Related Disorders via the TNNT2 Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy via the MYBPC3 Gene |
Sanger Sequencing |
$1380 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy via the MYL2 Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy via the MYL3 Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV PGxome |
$890 |
|
Hypertrophic Cardiomyopathy via the TNNC1 Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV PGxome |
$890 |
|
Hypochondroplasia via the FGFR3 Gene |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the AXL Gene |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the CCDC141 Gene |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the FEZF1 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the FGF17 Gene |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the FGF8 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the HS6ST1 Gene |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the IL17RD Gene |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the NSMF Gene |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the PROK2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the PROKR2 Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the SEMA3A Gene |
Sanger Sequencing |
$1250 |
Sequencing with CNV PGxome |
$890 |
|
Hypogonadotropic Hypogonadism/Kallmann Syndrome via the WDR11 Gene |
Sequencing with CNV PGxome |
$890 |
|
Hypomagnesemia via the FXYD2 Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV PGxome |
$890 |
|
Hypomyelination and Congenital Cataract (HCC) via the FAM126A Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV PGxome |
$890 |
|
Hypoparathyroidism, Sensorineural Deafness and Renal Disease (HDR) via the GATA3 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Hypophosphatasia via the ALPL Gene |
Sequencing with CNV PG-Select |
$640 |
|
Hypophosphatemia, X-Linked, via the PHEX Gene |
Sanger Sequencing |
$1190 |
Sequencing with CNV PGxome |
$890 |
|
Hypophosphatemic Nephrolithiasis/Osteoporosis-2 (NPHLOP2) via the SLC9A3R1 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Hypophosphatemic Rickets with Hypercalciuria via the SLC34A3 Gene |
Sanger Sequencing |
$990 |
Sequencing with CNV PGxome |
$890 |
|
Hypothyroidism [Congenital, Nongoitrous] and Hyperthyroidism [Familial Gestational & Nonautoimmune] via the TSHR Gene |
Sanger Sequencing |
$1020 |
Sequencing with CNV PGxome |
$890 |
|