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Results: 1 to 18 of 18

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Microphthalmia, syndromic type 1

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

X-linked Lenz Microphthalmia Syndrome and Lethal Ogden Syndrome via the NAA10 Gene

PreventionGenetics
United States
21
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Microphthalmia/Anophthalmia Disorders Panel

Invitae
United States
74
  • 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

Invitae Oculo-Facio-Cardio-Dental Syndrome Test

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

BCOR Remaining Exons Sequencing

GeneDx
United States
21
  • E Sequence analysis of select exons

Microphthalmia, syndromic 2

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

Microphthalmy Panel

CeGaT GmbH
Germany
1326
  • C Sequence analysis of the entire coding region

X-Linked Intellectual Disability Panel, Sequencing, 76 Genes

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
12776
  • C Sequence analysis of the entire coding region

NAA10

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

BCOR

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

devSEEKĀ® Sequence Analysis for Neurodevelopmental Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
261201
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

X-linked Intellectual Disability: Gene Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
13991
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

XLID NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
188107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Disorders NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
252138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lenz Microphthalmia Syndrome

Biesecker Lab/Human Development Section National Institutes of Health
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 18 of 18

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