Explore our tests
Discover the right genetic test for your patient in our complete list of tests and panels.
Showing 10 out of 411 tests
Hirschsprung Disease (Non-syndromic) Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10225
2 - 3 weeks (7 - 16 days STAT)•Test 102256 Genes
Holoprosencephaly, Autosomal Dominant, Nonsyndromic, Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 10317
2 - 3 weeks (7 - 16 days STAT)•Test 1031714 Genes
Holt-Oram Syndrome (HOS) via the TBX5 Gene
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 8475
2 - 3 weeks (7 - 16 days STAT)•Test 84751 Gene
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