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Results: 1 to 17 of 17
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
TSEN34 - 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 | 777 | 770 |
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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 Brain Malformations Panel Invitae United States | 247 | 161 |
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PreventionGenetics, part of Exact Sciences United States | 79 | 52 |
|
Pontocerebellar Hypoplasia Panel PreventionGenetics, part of Exact Sciences United States | 14 | 12 |
|
Pontocerebellar Hypoplasia via the TSEN34 Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
|
Fulgent Genetics United States | 509 | 275 |
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Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
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Fulgent Genetics United States | 1 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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Fulgent Genetics United States | 322 | 75 |
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Cerebellar Hypoplasia NGS Panel Fulgent Genetics United States | 10 | 8 |
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Pontocerebellar Hypoplasia NGS Panel Fulgent Genetics United States | 11 | 9 |
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Results: 1 to 17 of 17
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.