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Results: 1 to 20 of 120

Tests names and labsConditionsGenes, analytes, and microbesMethods

Achromatopsia

Molecular Genetics Laboratory Institute for Ophthalmic Research
Germany
76
  • C Sequence analysis of the entire coding region

Achromatopsia

Asper Biogene Asper Biogene LLC
Estonia
66
  • C Sequence analysis of the entire coding region

ACHROMATOPSIA

Laboratorio de Genetica Clinica SL
Spain
66
  • C Sequence analysis of the entire coding region

Achromatopsia

Amplexa Genetics Amplexa Genetics A/S
Denmark
110
  • S Mutation scanning of the entire coding region

Achromatopsia 3, 262300, Autosomal recessive; ACHM3 (Achromatopsia) (CNGB3 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

Achromatopsia 7, 616517, Autosomal recessive; ACHM7 (Achromatopsia) (ATF6 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

Achromatopsia 4, 613856; ACHM4 (Achromatopsia) (GNAT2 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

Achromatopsia 2, 216900, Autosomal recessive; ACHM2 (Achromatopsia) (CNGA3 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

Achromatopsia

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

Achromatopsia 6, 610024, Autosomal recessive, Autosomal dominant (Achromatopsia) (PDE6H 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

Achromatopsia Panel

CeGaT GmbH
Germany
106
  • C Sequence analysis of the entire coding region

Achromatopsia (ACHM) Panel

PreventionGenetics, part of Exact Sciences
United States
76
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Achromatopsia panel

Molecular Vision Laboratory
United States
86
  • C Sequence analysis of the entire coding region

Invitae Achromatopsia Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
78
  • D Deletion/duplication analysis

Achromatopsia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
55
  • C Sequence analysis of the entire coding region

Achromatopsia panel. 8-gene NGS panel.

Genologica Medica
Spain
88
  • C Sequence analysis of the entire coding region

CNGA3 Gene Achromatopsia type 2 NGS Genetic DNA Test

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

CNGB3 Gene Achromatopsia type 3 NGS Genetic DNA Test

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

GNAT2 Gene Achromatopsia type 4 NGS Genetic DNA Test

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

PDE6H Gene Achromatopsia type 6 NGS Genetic DNA Test

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

Results: 1 to 20 of 120

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.