Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
AASS Gene Hyperlysinemia type 1 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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AASS Gene Saccharopinuria NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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Molecular Vision Laboratory United States | 1358 | 1028 |
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AASS - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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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 |
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Invitae Nuclear Mitochondrial Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 394 | 319 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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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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Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 1 | 625 |
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MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
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CGC Genetics Unilabs Portugal | 1 | 837 |
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Movement diseases (WES based NGS panel of 931 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 10 | 930 |
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CGC Genetics Unilabs Portugal | 1 | 1307 |
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Parkinson's and movement disorders panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 256 |
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HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
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MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES) Laboratorio de Genetica Clinica SL Spain | 1 | 1372 |
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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.