Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Beacon Expanded Female Carrier Screening Panel Fulgent Genetics United States | 690 | 326 |
|
Nonsyndromic Autosomal Recessive retinitis pigmentosa: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 55 |
|
Nonsyndromic Autosomal Dominant Retinitis Pigmentosa: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 26 |
|
ENHANCED S-CONE SYNDROME (GOLDMANN - FAVRE DISEASE) Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Retinitis Pigmentosa NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 103 | 92 |
|
Blueprint Genetics Finland | 1 | 260 |
|
Blueprint Genetics Finland | 1 | 23 |
|
Blueprint Genetics Finland | 1 | 110 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 2 | 1 |
|
Molecular Vision Laboratory United States | 372 | 283 |
|
Retinitis pigmentosa, autosomal recessive and X-linked Panel CeGaT GmbH Germany | 37 | 62 |
|
Retinitis pigmentosa, autosomal dominant and X-linked Panel CeGaT GmbH Germany | 24 | 30 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Retinitis Pigmentosa NGS Panel Fulgent Genetics United States | 329 | 124 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
|
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.