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Results: 1 to 19 of 19

Tests names and labsConditionsGenes, analytes, and microbesMethods

Exudative vitreoretinopathy Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Exudative vitreoretinopathy NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
67
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Exudative vitreoretinopathy Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Exudative Vitreoretinopathy and Wagner Syndrome

Amplexa Genetics Amplexa Genetics A/S
Denmark
28
  • S Mutation scanning of the entire coding region

Exudative vitreoretinopathy NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
67
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Exudative vitreoretinopathy Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Exudative vitreoretinopathy Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Inherited Retinal Dystrophies Panel

PreventionGenetics, Part of Exact Sciences
United States
161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Exudative Vitreoretinopathy 1 (FEVR1) via the FZD4 Gene

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

Retinopathy and Optic Atrophy NGS Panel

Fulgent Genetics
United States
563241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Exudative Vitreoretinopathy, Autosomal Dominant: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
13
  • C Sequence analysis of the entire coding region

ZNF408 Single Gene

Fulgent Genetics
United States
321
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PRSS23 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ARHGAP1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Secuenciaci���³n

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

Familial exudative vitreoretinopathy

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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 19 of 19

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.