Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
CHRNB2 Gene Epilepsy, nocturnal frontal lobe type 3 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Comprehensive Epilepsy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 318 |
|
CHRNB2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 734 | 744 |
|
Molecular Genetics Laboratory London Health Sciences Centre Canada | 1 | 166 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Genomic Unity Epilepsy Analysis (includes STR analysis of 6 loci) Variantyx, Inc. United States | 1 | 378 |
|
Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 125 |
|
Epilepsy - Intellectual Disability - Autism Spectrum Disorder Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 600 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 466 | 297 |
|
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy via the CHRNB2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Baylor Genetics United States | 1 | 397 |
|
Baylor Genetics United States | 1 | 76 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
CGC Genetics Unilabs Portugal | 1 | 759 |
|
Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
|
Nocturnal frontal lobe epilepsy (WES based NGS panel of 8 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 8 |
|
Epilepsies (deletion/duplication analysis on CHRNA4, CHRNB2, EPM2A, KCNQ1, KCNQ3 and NHLRC1 genes) CGC Genetics Unilabs Portugal | 1 | 6 |
|
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