Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 2 | 1 |
|
CeGaT GmbH Germany | 2 | 16 |
|
CeGaT GmbH Germany | 2 | 16 |
|
Zellweger syndrome, PEX1 sequencing Molecular Diagnostics Laboratory Seoul National University Hospital South Korea | 1 | 1 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 121 | 66 |
|
Fulgent Genetics United States | 5130 | 4674 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Fulgent Genetics United States | 20 | 12 |
|
Retinitis Pigmentosa NGS Panel Fulgent Genetics United States | 329 | 124 |
|
Fulgent Genetics United States | 77 | 21 |
|
Fulgent Genetics United States | 280 | 112 |
|
Fulgent Genetics United States | 186 | 106 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
|
Peroxisome biogenesis disorder 1A (Zellweger) Praxis fuer Humangenetik Wien Austria | 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.