Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
EHLERS-DANLOS SYNDROME WITH HETEROTOPIA PERIVENTRICULAR Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Periventricular Nodular Heterotopia, Sequencing FLNA Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Comprehensive Pulmonary-Vascular Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 100 | 86 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 36 | 32 |
|
Asper Biogene Asper Biogene LLC Estonia | 210 | 204 |
|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
Asper Biogene Asper Biogene LLC Estonia | 38 | 24 |
|
X-linked periventricular nodular heterotopia Bioarray Spain | 1 | 1 |
|
Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 158 | 165 |
|
CeGaT GmbH Germany | 9 | 1 |
|
Fulgent Genetics United States | 9 | 1 |
|
Ehlers-Danlos Syndrome NGS Panel Fulgent Genetics United States | 97 | 21 |
|
Fulgent Genetics United States | 543 | 178 |
|
Asper Biogene Asper Biogene LLC Estonia | 166 | 74 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
XLID (X-Linked Intellectual Disability) NGS Panel Fulgent Genetics United States | 162 | 117 |
|
Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
|
Fulgent Genetics United States | 187 | 60 |
|
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States | 671 | 250 |
|
Marfan Syndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel Fulgent Genetics United States | 65 | 31 |
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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.