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Other countries
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
KCNV2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 417 | 413 |
|
Invitae Macular Dystrophy Panel Invitae United States | 66 | 36 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
|
Molecular Vision Laboratory United States | 342 | 268 |
|
Cone-Rod Dystrophy via the KCNV2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 37 | 35 |
|
Baylor Genetics United States | 842 | 637 |
|
Retinal cone dystrophy type 3B (sequence analysis of KCNV2 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Rod and cone dystrophy panel. 42-gene NGS panel. Genologica Medica Spain | 65 | 41 |
|
Retinal dystrophy panel. 260 gene NGS panel. Genologica Medica Spain | 420 | 257 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States | 563 | 241 |
|
Cone Rod Distrophy , Panel Massive Sequencing (NGS) 30 Genes Reference Laboratory Genetics Spain | 29 | 30 |
|
Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 45 | 37 |
|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
CeGaT GmbH Germany | 1 | 1 |
|
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.