| Galactosemia Type I (Classic and Variant Galactosemia) via the GALT Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV
PGxome |
$890 |
|
| Galactosemia Type I (Classic and Variant Galactosemia) via the GALT Gene, 5.5 kb Common Deletion |
|
| Galactosemia Type II (Galactokinase Deficiency) via the GALK1 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV
PGxome |
$890 |
|
| Galactosialidosis via the CTSA Gene |
Sanger Sequencing |
$990 |
Sequencing with CNV
PGxome |
$890 |
|
| Galloway-Mowat Syndrome (GAMOS) via the GON7 Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Galloway-Mowat Syndrome (GAMOS) via the LAGE3 Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV
PGxome |
$890 |
|
| Galloway-Mowat Syndrome (GAMOS) via the OSGEP Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Galloway-Mowat Syndrome (GAMOS) via the TP53RK Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV
PGxome |
$890 |
|
| Galloway-Mowat Syndrome (GAMOS) via the TPRKB Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Galloway-Mowat Syndrome (GAMOS) via the WDR73 Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV
PGxome |
$890 |
|
| GAPO Syndrome via the ANTXR1 Gene |
Sanger Sequencing |
1,100 |
Sequencing with CNV
PGxome |
$890 |
|
| Gaucher Disease via the GBA Gene |
|
| GDF5-related Disorders via the GDF5 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Gelatinous Drop-Like Corneal Dystrophy (GDLD) via the TACSTD2 Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV
PGxome |
$890 |
|
| Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum (PXE) via the ABCC6 Gene |
Sequencing with CNV
PG-Select |
$1870 |
|
| Generalized Arterial Calcification of Infancy via the ENPP1 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Generalized Epilepsy with Febrile Seizures Plus and Dravet syndrome via the SCN1B Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Generalized Epilepsy With Febrile Seizures Plus via the GABRG2 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Genitourinary and/or Brain Malformation Syndrome (GUBS) via the PPP1R12A Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Geroderma Osteodysplasticum (GO) via the GORAB Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Giant Axonal Neuropathy via the GAN Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV
PGxome |
$890 |
|
| Gitelman Syndrome via the SLC12A3 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Glanzmann's Thrombasthenia via the ITGA2B Gene |
Sanger Sequencing |
$1220 |
Sequencing with CNV
PGxome |
$890 |
|
| Glanzmann's Thrombasthenia via the ITGB3 Gene |
Sanger Sequencing |
$970 |
Sequencing with CNV
PGxome |
$890 |
|
| Globozoospermia via the SPATA16 Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV
PGxome |
$890 |
|
| Glomerulopathy with Fibronectin Deposits via the FN1 Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Glucose Phosphate Isomerase Deficiency via the GPI Gene |
Sanger Sequencing |
$1060 |
Sequencing with CNV
PGxome |
$890 |
|
| Glucose-6-Phosphate Dehydrogenase Deficiency via the G6PD Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| GLUT1 Deficiency Syndrome via the SLC2A1 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Glutaric Acidemia Type I via the GCDH Gene |
Sanger Sequencing |
$790 |
Sequencing with CNV
PGxome |
$890 |
|
| Glutaric Acidemia Type II via the ETFA Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV
PGxome |
$890 |
|
| Glutaric Acidemia Type II via the ETFB Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV
PGxome |
$890 |
|
| Glutaric Acidemia Type II via the ETFDH Gene |
Sanger Sequencing |
$910 |
Sequencing with CNV
PGxome |
$890 |
|
| Glutathione Synthetase Deficiency via the GSS Gene |
Sanger Sequencing |
$910 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycine Encephalopathy via the GCSH Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Glycine N-Methyltransferase Deficiency via the GNMT Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type 0 via the Glycogen Synthase 2 (GYS2) Gene |
Sanger Sequencing |
$1100 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type Ia via the G6PC Gene |
Sanger Sequencing |
$590 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type Ib via the SLC37A4 (G6PT1) Gene |
Sanger Sequencing |
$670 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type II (Pompe Disease) via the GAA Gene |
Sanger Sequencing |
$910 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type II (Pompe Disease) via the GAA Gene, Exon 18 Deletion |
|
| Glycogen Storage Disease Type III via the AGL Gene |
Sanger Sequencing |
$1590 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type IV via the GBE1 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Glycogen Storage Disease Type IX via the PHKA1 Gene |
Sanger Sequencing |
$1650 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type IX via the PHKA2 Gene |
Sanger Sequencing |
$1540 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type IX via the PHKB Gene |
Sanger Sequencing |
$1540 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type IX via the PHKG2 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type VI via the PYGL Gene |
Sanger Sequencing |
$990 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease Type VII (Tarui Disease) via the PFKM Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Glycogen Storage Disease Type X via the PGAM2 Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV
PGxome |
$890 |
|
| Glycogen Storage Disease, Type V (McArdle Disease) via the PYGM Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Glycyl tRNA Synthetase-Related Disorders via the GARS Gene |
Sanger Sequencing |
$940 |
Sequencing with CNV
PGxome |
$890 |
|
| GM1 Gangliosidosis and Mucopolysaccharidosis Type IVB / Morquio Type B via the GLB1 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| GM2-Gangliosidosis Variant AB via the GM2A Gene |
Sanger Sequencing |
$370 |
Sequencing with CNV
PGxome |
$890 |
|
| GM3 Synthase Deficiency via the ST3GAL5 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Gnathodiaphyseal Dysplasia via the ANO5 Gene |
Sanger Sequencing |
$1090 |
Sequencing with CNV
PGxome |
$890 |
|
| Goldberg-Shprintzen Megacolon Syndrome via the KIFBP (KIAA1279/KIF1BP) Gene |
Sanger Sequencing |
$810 |
Sequencing with CNV
PGxome |
$890 |
|
| Gray Platelet Syndrome via the NBEAL2 Gene |
Sanger Sequencing |
$2160 |
Sequencing with CNV
PGxome |
$890 |
|
| Griscelli Syndrome-Type 2 (GS2) via the RAB27A Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV
PGxome |
$890 |
|
| Gyrate Atrophy of Choroid and Retina via the OAT Gene |
Sanger Sequencing |
$810 |
Sequencing with CNV
PGxome |
$890 |
|
ORDER