Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Syndromic Hirschsprung Disease: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 28 |
|
Bardet-Biedl Syndrome NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 24 | 26 |
|
Laboratorio de Genetica Clinica SL Spain | 17 | 23 |
|
Blueprint Genetics Finland | 1 | 260 |
|
Blueprint Genetics Finland | 2 | 23 |
|
Blueprint Genetics Finland | 6 | 99 |
|
Monogenic causes of nephronophthisis and related ciliopathies Hildebrandt Laboratory Boston Children's Hospital United States | 7 | 93 |
|
Molecular Vision Laboratory United States | 38 | 23 |
|
Molecular Vision Laboratory United States | 372 | 283 |
|
CeGaT GmbH Germany | 17 | 24 |
|
CeGaT GmbH Germany | 17 | 24 |
|
CeGaT GmbH Germany | 17 | 24 |
|
Genetic Services Laboratory University of Chicago United States | 1 | 22 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5124 | 4672 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1017 | 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.