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
Cornelia de Lange Syndrome and Related Disorders Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 10399
42 Genes
Craniofacial Malformations Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 10343
19 Genes
Craniosynostosis and Related Disorders Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 10197
5 Genes
Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene
NGS with CNV (PGselect Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 7851
1 Gene
Currarino Syndrome via the MNX1 Gene
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 9829
1 Gene
CYP21A2 Whole Gene Duplication Test
Targeted PCR
2 - 3 weeks (8 - 10 days STAT)•Test 16165
1 Gene
Cystic Fibrosis and CF-Related Disorders via the CFTR Gene
NGS with CNV (PGselect Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 3035
1 Gene
Cystinosis via the CTNS Gene, 57-kb Deletion
Targeted PCR
2 - 3 weeks (8 - 10 days STAT)•Test 1636
1 Gene
Cystinuria Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10075
2 Genes
Deafness, Autosomal Recessive 16 (DFNB16) via MLPA of STRC
Multiplex Ligation-Dependent Probe Amplification Assay
2 - 3 weeks (6 - 11 days STAT)•Test 12548
1 Gene