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Results: 1 to 18 of 18
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Caudal regression syndrome (deletion/duplication analysis on VANGL1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
WDR45B - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 734 | 744 |
|
Centogene AG - the Rare Disease Company Germany | 669 | 688 |
|
Ataxia / Spastic Paraplegia Comprehensive Panel Centogene AG - the Rare Disease Company Germany | 451 | 452 |
|
Ataxia / Spastic Paraplegia Panel Centogene AG - the Rare Disease Company Germany | 442 | 443 |
|
qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
|
CGC Genetics Unilabs Portugal | 1 | 759 |
|
Hereditary Spastic Paraplegia Panel CGC Genetics Unilabs Portugal | 1 | 97 |
|
CGC Genetics Unilabs Portugal | 1 | 1307 |
|
Epileptic encephalopathy (WES based NGS panel of 137 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 137 |
|
Mendelics Brazil | 1 | 240 |
|
HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 1501 |
|
Fulgent Genetics United States | 1 | 1 |
|
Results: 1 to 18 of 18
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.