Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
GCSH Gene Glycine encephalopathy NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Genomic Unity® Nuclear Encoded Mitochondrial Gene Analysis Variantyx, Inc. United States | 1 | 335 |
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Centogene AG - the Rare Disease Company Germany | 316 | 314 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 669 | 688 |
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Centogene AG - the Rare Disease Company Germany | 406 | 414 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
PreventionGenetics, part of Exact Sciences United States | 11 | 11 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
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Genomic Unity Epilepsy Analysis (includes STR analysis of 6 loci) Variantyx, Inc. United States | 1 | 378 |
|
Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 1 | 625 |
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Epilepsy - Intellectual Disability - Autism Spectrum Disorder Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 600 |
|
Glycine Encephalopathy via the GCSH Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
CGC Genetics Unilabs Portugal | 1 | 837 |
|
CGC Genetics Unilabs Portugal | 1 | 759 |
|
Epileptic encephalopathy (WES based NGS panel of 137 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 137 |
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CGC Genetics Unilabs Portugal | 1 | 3 |
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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.