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
3-Methylcrotonyl-CoA Carboxylase Deficiency Panel
Sequencing with CNV PGxome
2 - 3 weeks (6 - 12 days STAT)•Test 10069
2 Genes
Adams-Oliver Syndrome Panel
Sequencing with CNV PGxome
2 - 3 weeks (7 - 16 days STAT)•Test 13027
8 Genes
Adrenocortical Carcinoma (ACC) Panel
Sequencing with CNV PG-Select
2 - 3 weeks (7 - 16 days STAT)•Test 16213
8 Genes
Alagille Syndrome Panel
Sequencing with CNV PGxome
2 - 3 weeks (7 - 16 days STAT)•Test 10071
2 Genes
Allan-Herndon-Dudley Syndrome or Monocarboxylate Transporter 8 Deficiency via the SLC16A2 Gene
Sequencing with CNV PGxome
N/A•Test 8515
1 Gene
Alnylam Act® Acute Hepatic Porphyria Sponsored Testing Program
Sponsored TestNGS with CNV (Exome or Genome Platform)
2 - 3 weeks•Test 16301
10 Genes
Alnylam Act® hATTR Amyloidosis Sponsored Testing Program
Sponsored TestNGS with CNV (Exome or Genome Platform)
2 - 3 weeks•Test 15139
1 Gene
Alnylam Act® Primary Hyperoxaluria Type 1 Sponsored Testing Program
Sponsored TestNGS with CNV (Exome or Genome Platform)
2 - 3 weeks•Test 16035
45 Genes
Alnylam Act® Primary Hyperoxaluria Type 1 Sponsored Testing Program
Sponsored TestNGS with CNV (Exome or Genome Platform)
2 - 3 weeks•Test 16029
3 Genes
Alpha Thalassemia Deletion/Duplication and Constant Spring Panel
MLPA
2 - 3 weeks (6 - 11 days STAT)•Test 6070
2 Genes