Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 1 to 20 of 105

Tests names and labsConditionsGenes, analytes, and microbesMethods

New Born testing (CentoICU)

Centogene AG - the Rare Disease Company
Germany
767514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7851205
  • C Sequence analysis of the entire coding region

Epilepsy Expanded Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1191
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Encephalopathy with Seizures Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1129
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Progressive Myoclonic Epilepsy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early Epileptic Encephalopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
190
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

EpiPanelDx PLUS

Lineagen, Inc
United States
3243
  • E Sequence analysis of select exons

Epilepsy Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
1166
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy and Seizure Panel

PreventionGenetics
United States
485374
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Epilepsy and Seizure Plus Panel

PreventionGenetics
United States
285198
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), 254800, Autosomal recessive (Unverricht-Lundborg disease)(Repeat Analysis)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • T Targeted variant analysis

Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), 254800, Autosomal recessive (Unverricht-Lundborg disease) (Prenatal)(Repeat Analysis)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • T Targeted variant analysis

Invitae Mendelian Disorders with Psychiatric Symptoms Panel

Invitae
United States
247163
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genomic Unity Epilepsy Analysis (includes STR analysis of 5 loci)

Variantyx, Inc.
United States
1378
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

CHILDHOOD EPILEPSY

Amplexa Genetics Amplexa Genetics A/S
Denmark
1125
  • S Mutation scanning of the entire coding region

Progressive Myoclonic Epilpesy

Amplexa Genetics Amplexa Genetics A/S
Denmark
111
  • S Mutation scanning of the entire coding region

Epilepsy - Intellectual Disability - Autism Spectrum Disorder

Amplexa Genetics Amplexa Genetics A/S
Denmark
1600
  • S Mutation scanning of the entire coding region

Epilepsy: Unverricht-Lundborg Disease via the CSTB Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ataxia Exome

Genetic Services Laboratory University of Chicago
United States
289481
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 105

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.

Support Center