Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
HPCA Gene DYT2 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Invitae Cerebral Palsy Spectrum Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 638 | 419 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Genetic Services Laboratory University of Chicago United States | 93 | 170 |
|
Invitae Dystonia Comprehensive Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 61 | 38 |
|
Cerebral Palsy Spectrum Disorders Panel Baylor Genetics United States | 1 | 419 |
|
Movement diseases (WES based NGS panel of 931 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 10 | 930 |
|
Parkinson's and movement disorders panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 256 |
|
Dystonia (WES based NGS panel of 117 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 117 |
|
Torsion dystonia 2 (DYT2, sequence analysis of HPCA gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Torsion dystonia 2 (DYT2, deletion/duplication analysis on HPCA gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 119 |
|
Codex Genetics Limited Hong Kong | 1 | 490 |
|
GeneDx United States | 1 | 83 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Xpanded Adult Movement Disorders Panel GeneDx United States | 5 | 473 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 999 |
|
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.