Explore our tests
Discover the right genetic test for your patient in our complete list of tests and panels.
Showing 10 out of 407 tests
Homocystinuria via the CBS Gene
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 9369
2 - 3 weeks (7 - 16 days STAT)•Test 93691 Gene
Huntington Disease via the HTT CAG Repeat Expansion
Repeat-Primed PCR & Fragment Length1 - 2 weeks (6 - 10 days STAT)•Test 2299
1 - 2 weeks (6 - 10 days STAT)•Test 22991 Gene
Hydrocephalus Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 7939
2 - 3 weeks (7 - 16 days STAT)•Test 793938 Genes
Hyperammonemia Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 10407
2 - 3 weeks (7 - 16 days STAT)•Test 1040763 Genes
Hypermethioninemia Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 10133
2 - 3 weeks (7 - 16 days STAT)•Test 101334 Genes
Hyperphenylalaninemia Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 3403
2 - 3 weeks (7 - 16 days STAT)•Test 34036 Genes
Hyperphenylalaninemia/Phenylalanine Hydroxylase Deficiency via the PAH Gene
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 9725
2 - 3 weeks (7 - 16 days STAT)•Test 97251 Gene
Hypertrophic Cardiomyopathy Panel
NGS with CNV (Exome or Genome Platform) 2 - 3 weeks (7 - 16 days STAT)•Test 1313
2 - 3 weeks (7 - 16 days STAT)•Test 131368 Genes
Hypoglycemia Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 12057
2 - 3 weeks (7 - 16 days STAT)•Test 12057171 Genes
Hypogonadotropic Hypogonadism/Kallmann Syndrome Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (6 - 12 days STAT)•Test 5243
2 - 3 weeks (6 - 12 days STAT)•Test 524338 Genes