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
Extract and Hold
Sequencing with CNV PGxome
3 weeks (STAT 2 weeks)•Test 14033
3 weeks (STAT 2 weeks)•Test 14033Fabry Disease via the GLA Gene
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 7681
2 - 3 weeks (7 - 16 days STAT)•Test 76811 Gene
Factor VII Deficiency via the F7 Gene
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 4149
2 - 3 weeks (7 - 16 days STAT)•Test 41491 Gene
Familial Amyloidosis (hATTR) via the TTR Gene
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 8983
2 - 3 weeks (7 - 16 days STAT)•Test 89831 Gene
Familial Chylomicronemia Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (6 - 12 days STAT)•Test 13025
2 - 3 weeks (6 - 12 days STAT)•Test 130257 Genes
Familial Hemiplegic Migraine Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 10161
2 - 3 weeks (7 - 16 days STAT)•Test 101618 Genes
Familial Hemophagocytic Lymphohistiocytosis (FHL) Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (6 - 12 days STAT)•Test 10377
2 - 3 weeks (6 - 12 days STAT)•Test 1037729 Genes
Familial Hemophagocytic Lymphohistiocytosis-Type 3 (FHL3) via the UNC13D Inversion
Targeted PCR2 - 3 weeks (8 - 10 days STAT)•Test 2050
2 - 3 weeks (8 - 10 days STAT)•Test 20501 Gene
Familial Hypercholesterolemia (FH) Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 10163
2 - 3 weeks (7 - 16 days STAT)•Test 101638 Genes
Familial Hypocalciuric Hypercalcemia (FHH) Panel
NGS with CNV (Exome or Genome Platform)2 - 3 weeks (7 - 16 days STAT)•Test 10125
2 - 3 weeks (7 - 16 days STAT)•Test 101253 Genes