Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Holoprosencephaly, Panel Massive Sequencing (NGS) 8 Genes Reference Laboratory Genetics Spain | 8 | 8 |
|
Holoprosencephaly Type 7 , Sequencing PTCH1 Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Comprehensive Hereditary Cancer Panel Baylor Genetics United States | 132 | 61 |
|
Hereditary Brain, CNS, PNS Cancer Panel Baylor Genetics United States | 43 | 17 |
|
Hereditary Brain, CNS, PNS Cancer Panel Baylor Genetics United States | 43 | 17 |
|
Fulgent Genetics United States | 70 | 26 |
|
Full Comprehensive Cancer Panel Fulgent Genetics United States | 329 | 127 |
|
Nervous System / Brain Cancer Comprehensive Panel Fulgent Genetics United States | 133 | 27 |
|
Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
|
GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 8 | 12 |
|
Holoprosencephaly 7: PTCH1 gene sequence analysis GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 1 | 1 |
|
PTCH1 Gene Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 3 | 1 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 3 | 1 |
|
CeGaT GmbH Germany | 11 | 7 |
|
CeGaT GmbH Germany | 11 | 7 |
|
Overgrowth and Intellectual Disability NGS and Deletion/Duplication panel DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 20 | 13 |
|
Fulgent Genetics United States | 3 | 1 |
|
Fulgent Genetics United States | 13 | 7 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
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.