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Results: 1 to 20 of 62

Tests names and labsConditionsGenes, analytes, and microbesMethods

Choroideremia, 303100, X-linked dominant; CHM (Choroideremia) (CHM gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Choroideremia, 303100, X-linked dominant; CHM (Choroideremia) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

CHOROIDEREMIA

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Choroideremia

Asper Biogene Asper Biogene LLC
Estonia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Choroideremia

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

Choroideremia

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Choroideremia

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

CHM Gene Choroideremia NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Choroideremia via the CHM 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

X-linked Retinitis Pigmentosa (XLRP) and Choroideremia Panel

PreventionGenetics, part of Exact Sciences
United States
74
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Choroideremia (CHM Single Gene Test)

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

Choroideremia: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Choroideremia, X-Linked

Dep. of Paediatrics and Inherited Metabolic Disorders General University Hospital in Prague and First Faculty of Medicine, Charles University in Prague
Czech Republic
11
  • C Sequence analysis of the entire coding region

Choroideremia , Retinitis pigmentosa X-linked (deletion/duplication analysis on CHM, RPGR and RP2 gene)

CGC Genetics Unilabs
Portugal
13
  • D Deletion/duplication analysis

Choroideremia (sequence analysis of CHM gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

High-Resolution Rapid Microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

CentoScreen

Centogene AG - the Rare Disease Company
Germany
316314
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CHM - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 62

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.