Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
KRAS, BRAF, NRAS and MSI Mutation Analysis PathGroup United States | 23 | 3 |
|
IntelligeneCG LLC United States | 14 | 15 |
|
Invitae First Tier Population Screen Invitae United States | 10 | 11 |
|
Variant Resolution Test for ColoNext® (+RNAinsight®) Ambry Genetics United States | 48 | 10 |
|
Ambry Genetics United States | 48 | 20 |
|
MLH1/MSH2/MSH6/PMS2/EPCAM Somatic Tumor MMR Sequencing and Deletion/Duplication Test Impact Genetics Dynacare/LabCorp Canada | 6 | 5 |
|
Color Diagnostics, LLC DBA Color Health United States | 24 | 29 |
|
Baylor Genetics United States | 842 | 637 |
|
TP53 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 9 | 1 |
|
Baylor Genetics United States | 9 | 1 |
|
TP53 Deletion/Duplication Analysis Baylor Genetics United States | 9 | 1 |
|
TP53 Comprehensive - Sequence & Deletion/Duplication Analysis Baylor Genetics United States | 9 | 1 |
|
Color Diagnostics, LLC DBA Color Health United States | 51 | 59 |
|
Hereditary Colorectal Cancer Panel Mendelics Brazil | 1 | 42 |
|
Myriad Genetics, Inc. United States | 32 | 45 |
|
Dhiti Omics Technologies Private Ltd India | 136 | 84 |
|
Hereditary Colorectal Cancer Panel (20 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States | 10 | 20 |
|
Guideline Based Hereditary Cancer Panel (32 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States | 20 | 32 |
|
Comprehensive Hereditary Cancer Panel (66 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States | 35 | 66 |
|
NxGen MDx United States | 32 | 32 |
|
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.