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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Mitochondrial Genome Sequencing and Depletion/Integrity Panel Molecular Genetics Laboratory London Health Sciences Centre Canada | 47 | 52 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
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MGME1 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
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Ataxia / Spastic Paraplegia Comprehensive Panel Centogene US, LLC - The Rare Disease Company United States | 451 | 452 |
|
Ataxia / Spastic Paraplegia Panel Centogene US, LLC - The Rare Disease Company United States | 442 | 443 |
|
Centogene US, LLC - The Rare Disease Company United States | 669 | 688 |
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Centogene US, LLC - The Rare Disease Company United States | 406 | 414 |
|
Centogene US, LLC - The Rare Disease Company United States | 1886 | 1858 |
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Centogene US, LLC - The Rare Disease Company United States | 734 | 744 |
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MGME1 - 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 | 734 | 744 |
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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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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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Invitae Rhabdomyolysis and Metabolic Myopathy Panel Invitae United States | 202 | 128 |
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Invitae Nuclear Mitochondrial Disorders Panel Invitae United States | 394 | 319 |
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Mitochondrial Disorders Panel (Nuclear Genes Only) PreventionGenetics United States | 290 | 251 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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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.