Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Comprehensive Aortopathy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 54 | 48 |
|
Ehlers-Danlos Syndrome Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 28 | 22 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Centogene US, LLC - The Rare Disease Company United States | 316 | 314 |
|
Centogene US, LLC - The Rare Disease Company United States | 110 | 112 |
|
Centogene US, LLC - The Rare Disease Company United States | 740 | 728 |
|
Connective Tissue and Related Disorder Panel Centogene US, LLC - The Rare Disease Company United States | 75 | 76 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
Carrier Screening Guidelines-Based Panel Ambry Genetics United States | 199 | 165 |
|
Carrier Screening Ashkenazi Jewish Panel Ambry Genetics United States | 51 | 48 |
|
Connective Tissue and Related Disorder Panel Centogene AG - the Rare Disease Company Germany | 75 | 76 |
|
Centogene AG - the Rare Disease Company Germany | 110 | 112 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
PreventionGenetics United States | 285 | 137 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Invitae Comprehensive Carrier Screen without X-linked Disorders Invitae United States | 228 | 279 |
|
Invitae Comprehensive Carrier Screen Invitae United States | 247 | 301 |
|
Connective Tissue Disorders Panel PreventionGenetics United States | 164 | 99 |
|
Invitae Ehlers-Danlos Syndrome Panel Invitae United States | 38 | 17 |
|
Quantitative Genomic Medicine Laboratories, SL Spain | 328 | 300 |
|
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.