Filters

See more specimen types...

Other countries

Results: 1 to 20 of 30

Tests names and labsConditionsGenes and analytesMethods

Comprehensive Inherited Retinal Dystrophies (includes RPGR ORF15) Sequencing Panel

PreventionGenetics
United States
300280
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TREX1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres Syndrome 1 - TREX1 Del/Dup Analysis

Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
United States
41
  • D Deletion/duplication analysis

Aicardi-Goutieres Syndrome 1 - TREX1 Sequencing

Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
United States
41
  • C Sequence analysis of the entire coding region

TREX1

Institute for Human Genetics University Clinic Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

Retinal Vasculopathy with Cerebral Leukodystrophy , Sequencing TREX1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
351275
  • C Sequence analysis of the entire coding region

Invitae Primary Immunodeficiency Panel

Invitae
United States
282207
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Monogenic Autoimmunity Panel

Invitae
United States
10973
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Immune Dysregulation Disorders Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
3223
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres Syndrome Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
3312
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TREX1 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
41
  • C Sequence analysis of the entire coding region

Epileptic encephalopathies

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3535
  • C Sequence analysis of the entire coding region

Single gene testing TREX1

CeGaT GmbH
Germany
41
  • C Sequence analysis of the entire coding region

Vascular and lymphatic disorders Panel

CeGaT GmbH
Germany
1818
  • C Sequence analysis of the entire coding region

Vasculopathy, retinal, with cerebral leukodystrophy

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372287
  • C Sequence analysis of the entire coding region

Small vessel disease Panel

CeGaT GmbH
Germany
116
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy and differential diagnoses Panel

CeGaT GmbH
Germany
69175
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 30

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