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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
FXN - 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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Ataxia / Spastic Paraplegia Comprehensive Panel Centogene AG - the Rare Disease Company Germany | 451 | 452 |
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Ataxia / Spastic Paraplegia Panel Centogene AG - the Rare Disease Company Germany | 442 | 443 |
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Friedreich ataxia, 229300, Autosomal recessive (Friedreich ataxia) (MLPA) 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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Ambry Genetics United States | 58 | 30 |
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Ambry Genetics United States | 58 | 30 |
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Ambry Genetics United States | 236 | 167 |
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Ambry Genetics United States | 138 | 56 |
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Ambry Genetics United States | 189 | 92 |
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Baylor Genetics United States | 842 | 637 |
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Fulgent Genetics United States | 505 | 132 |
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Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States | 450 | 128 |
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Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
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Fulgent Genetics United States | 133 | 56 |
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Fulgent Genetics United States | 533 | 149 |
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Friedreich Ataxia, Deletions-Duplications (MLPA) FXN Gene Reference Laboratory Genetics Spain | 1 | 1 |
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Ataxia, Comprehensive Evaluation Athena Diagnostics Inc United States | 44 | 42 |
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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.