Filters

See more specimen types...

Other countries

Results: 1 to 16 of 16 (representing 12 labs)

Tests names and labsConditionsGenes and analytesMethods

Cataract, autosomal recessive congenital nuclear type 2

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

Cataract panel

Centogene AG - the Rare Disease Company
Germany
4845
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Cataracts Sequencing Panel

PreventionGenetics
United States
4340
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

FYCO1. Complete sequencing

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

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
845637
  • D Deletion/duplication analysis

Cataract Panel

Blueprint Genetics
Finland
154
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Diseases - panels

Medizinisch Genetisches Zentrum München MGZ München
Germany
6167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Congenital Cataracts Panel

Invitae
United States
4737
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FYCO1 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • C Sequence analysis of the entire coding region

Cataract 18, autosomal recessive

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

Cataracts (NGS panel for 41 genes)

CGC Genetics
Portugal
141
  • C Sequence analysis of the entire coding region

Cataract 18, AR (sequence analysis of FYCO1 gene)

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

Cataract Panel

CeGaT GmbH
Germany
2441
  • C Sequence analysis of the entire coding region

Congenital Cataract, Autosomal Recessive NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
2015
  • C Sequence analysis of the entire coding region

Cataract

Medizinisch Genetisches Zentrum München MGZ München
Germany
265
  • C Sequence analysis of the entire coding region

FYCO1

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

Results: 1 to 16 of 16

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