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Results: 1 to 20 of 24

Tests names and labsConditionsGenes, analytes, and microbesMethods

Signal PanCancer Panel

Sema4
United States
12196
  • D Deletion/duplication analysis
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Corneal dystrophy, posterior polymorphous, 3, 609141; PPCD3 (Posterior polymorphous corneal dystrophy) (ZEB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Corneal dystrophy, Fuchs endothelial, 6, 613270; FECD6 (Fuchs endothelial corneal dystrophy) (ZEB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

ZEB1-Associated Corneal Dystrophies via the ZEB1 Gene

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

Corneal Dystrophies Panel

PreventionGenetics
United States
3926
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
843637
  • D Deletion/duplication analysis

Corneal abnormalities (WES based NGS panel of 33 genes, including CNV analysis)

CGC Genetics
Portugal
133
  • C Sequence analysis of the entire coding region

Genomic Unity Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Xpanded Panel

GeneDx
United States
20856
  • C Sequence analysis of the entire coding region

ZEB1

Institute for Human Genetics University Clinic Freiburg
Germany
21
  • C Sequence analysis of the entire coding region

Corneal dystrophy, posterior polymorphous: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Corneal dystrophy, Fuchs endothelial: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Corneal Dystrophy NGS Panel

Fulgent Genetics
United States
4724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Posterior Polymorphous Corneal Dystrophy , Panel Massive Sequencing (NGS) OVOL2, COL8A2, ZEB1

Reference Laboratory Genetics
Spain
33
  • C Sequence analysis of the entire coding region

Corneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes

Reference Laboratory Genetics
Spain
2718
  • C Sequence analysis of the entire coding region

POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY

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

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
369292
  • C Sequence analysis of the entire coding region

Corneal Dystrophy Panel

Blueprint Genetics
Finland
127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Diseases - panels

MGZ Medical Genetics Center
Germany
6167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Posterior polymorphous corneal dystrophy 3 (PPCD3): ZEB1 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 24

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