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
Congenital Adrenal Hyperplasia (CAH) Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 12053
7 Genes
Congenital Adrenal Hyperplasia (CAH) via the CYP21A2 Gene
Sanger Sequencing
3 - 4 weeks (12 - 20 days STAT)•Test 1419
1 Gene
Congenital Anomalies of the Gastrointestinal Tract Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 13377
180 Genes
Congenital Central Hypoventilation Syndrome (CCHS) Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10239
7 Genes
Congenital Central Hypoventilation Syndrome (CCHS) via the PHOX2B Gene
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 8967
Congenital Defects of Phagocytes Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 16091
43 Genes
Congenital Diaphragmatic Hernia Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 13359
65 Genes
Congenital Diarrhea and Enteropathies Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 12647
157 Genes
Congenital Disorders of Glycosylation (CDG) Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 10625
54 Genes
Congenital Fibrinogen Deficiency Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10119
3 Genes