Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Brugada syndrome and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 18 | 26 |
|
Cardiac channelopathy Deletion/ Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 1 | 41 |
|
Brugada syndrome and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 18 | 26 |
|
Brugada syndrome and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 18 | 26 |
|
Genetic Services Laboratory University of Chicago United States | 289 | 481 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 466 | 297 |
|
Early Infantile Epileptic Encephalopathy Panel PreventionGenetics, part of Exact Sciences United States | 144 | 124 |
|
Early Infantile Epileptic Encephalopathy Panel Genetic Services Laboratory University of Chicago United States | 47 | 125 |
|
Baylor Genetics United States | 1 | 397 |
|
Cerebral Palsy Spectrum Disorders Panel Baylor Genetics United States | 1 | 419 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
CGC Genetics Unilabs Portugal | 1 | 759 |
|
CGC Genetics Unilabs Portugal | 1 | 1307 |
|
Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
|
Brugada syndrome (WES based NGS panel of 23 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 23 |
|
Epileptic encephalopathy panel. 128-gene NGS panel. Genologica Medica Spain | 197 | 128 |
|
Complete epilepsy panel. NGS panel of 283 genes. Genologica Medica Spain | 409 | 283 |
|
Developmental and epileptic encephalopathy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 91 | 90 |
|
Codex Genetics Limited Hong Kong | 1 | 490 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 145 |
|
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.