Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Fragile X Syndrome, Repeat Number Analysis with Reflex to Methylation Analysis Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States | 6 | 1 |
|
Fragile X Tremor-Ataxia Syndrome Genetics Laboratory Shodair Children's Hospital United States | 1 | 1 |
|
Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 185 | 145 |
|
Carrier Screening - Fragile X Syndrome (FMR1) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 3 | 1 |
|
Fragile X Syndrome, Mol. Analysis Mayo Clinic Laboratories Mayo Clinic United States | 4 | 1 |
|
Invitae FMR1-Fragile X Syndrome and Related Disorders Repeat Expansion Test Labcorp Genetics (formerly Invitae) LabCorp United States | 3 | 1 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 243 | 238 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
FMR1 - Repeat expansion analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Genomic UnityⓇ Ataxia Repeat Expansion Analysis (STR analysis of 16 loci) Variantyx, Inc. United States | 15 | 13 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 224 | 112 |
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Invitae Comprehensive Carrier Screen Labcorp Genetics (formerly Invitae) LabCorp United States | 886 | 547 |
|
Genetic Services Laboratory University of Chicago United States | 14 | 14 |
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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.