Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 185 | 145 |
|
F11 Gene Factor XI deficiency NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Hemophilia C, F11 Gene, Full Gene Next-Generation Sequencing Mayo Clinic Laboratories Mayo Clinic United States | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
F11 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Carrier Screening Guidelines-Based Panel Ambry Genetics United States | 199 | 164 |
|
Carrier Screening Ashkenazi Jewish Panel Ambry Genetics United States | 51 | 47 |
|
Centogene AG - the Rare Disease Company Germany | 110 | 112 |
|
Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
Factor XI deficiency, autosomal dominant, 612416 (Congenital factor XI deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 136 |
|
Quantitative Genomic Medicine Laboratories, SL Spain | 328 | 300 |
|
PreventionGenetics, part of Exact Sciences United States | 78 | 79 |
|
Molecular Haemostasis & Thrombosis Viapath - Guy's and St. Thomas' NHS Foundation Trust United Kingdom | 1 | 1 |
|
Coagulation Factor Deficiency Panel PreventionGenetics, part of Exact Sciences United States | 21 | 20 |
|
PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Factor XI Mutation Analysis (Ashkenazi Jewish) Quest Diagnostics Nichols Institute San Juan Capistrano United States | 1 | 1 |
|
Hematology Comprehensive Panel CGC Genetics Unilabs Portugal | 1 | 291 |
|
CGC Genetics Unilabs Portugal | 1 | 121 |
|
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.