Explore our tests
Discover the right genetic test for your patient in our complete list of tests and panels.
Showing 10 out of 402 tests
Hyperammonemia Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10407
63 Genes
Hypermethioninemia Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10133
4 Genes
Hyperphenylalaninemia Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 3403
6 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
1 Gene
Hypertrophic Cardiomyopathy Panel
Sequencing with CNV PGxome
2 - 3 weeks (7 - 16 days STAT)•Test 1313
68 Genes
Hypoglycemia Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 12057
171 Genes
Hypogonadotropic Hypogonadism/Kallmann Syndrome Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 5243
38 Genes
Hypomagnesemia Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 3025
16 Genes
Hypoparathyroidism Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 2653
28 Genes
Hypophosphatasia via the ALPL Gene
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 7573
1 Gene