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Results: 1 to 20 of 146

Tests names and labsConditionsGenes, analytes, and microbesMethods

Aniridia 2, 617141, Autosomal dominant; AN2 (Isolated aniridia) (ELP4 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

Aniridia 3, 617142, Autosomal dominant; AN3 (Isolated aniridia) (TRIM44 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

Aniridia, 106210, Autosomal dominant (Isolated aniridia) (MLPA)

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

Aniridia, 106210, Autosomal dominant (Isolated aniridia) (PAX6 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

Aniridia

Human Developmental Genetics Laboratory Medical College of Wisconsin
United States
13
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ANIRIDIA

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

Aniridia

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

Aniridia

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aniridia

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aniridia

Praxis fuer Humangenetik Wien
Austria
11
  • S Mutation scanning of the entire coding region

Aniridia

Institute of Human Genetics Cologne University
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aniridia

Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet
Denmark
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aniridia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
43
  • C Sequence analysis of the entire coding region

PAX6 Gene Aniridia NGS Genetic DNA Test

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

Aniridia (PAX6 Single Gene Test)

Fulgent Genetics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Gillespie syndrome, 206700; GLSP (Aniridia-cerebellar ataxia-intellectual disability syndrome) (ITPR1 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

Gillespie syndrome, 206700; GLSP (Aniridia-cerebellar ataxia-intellectual disability syndrome) (ITPR1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Aniridia testing (PAX6)

Genetic Services Laboratory University of Chicago
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aniridia via the PAX6 Gene

PreventionGenetics, part of Exact Sciences
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cataract with late-onset corneal dystrophy, 106210, Autosomal dominant (Isolated aniridia) (PAX6 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

Results: 1 to 20 of 146

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.