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Results: 61 to 80 of 88

Tests names and labsConditionsGenes, analytes, and microbesMethods

Neuro-Ophthalmic Disorders NGS Panel

Fulgent Genetics
United States
5226
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SOX2 Anophthalmia Syndrome (SOX2 Single Gene Test)

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

Retinopathy and Optic Atrophy NGS Panel

Fulgent Genetics
United States
563241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Gastrointestinal Atresia NGS Panel

Fulgent Genetics
United States
277
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel

Fulgent Genetics
United States
24478
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Esophageal Atresia/Tracheoesophageal Fistula: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
524
  • C Sequence analysis of the entire coding region

SOX2-Related Eye Disorders: gene deletion/duplication

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

SOX2-Related Eye Disorders: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Septo-Optic Dysplasia , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
119
  • C Sequence analysis of the entire coding region

Microphthalmia , Panel Massive Sequencing (NGS) 14 Genes

Reference Laboratory Genetics
Spain
1614
  • C Sequence analysis of the entire coding region

ANOPHTHALMIA/ MICROPHTALMIA

Laboratorio de Genetica Clinica SL
Spain
79
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Septo-Optic Dysplasia , Sequencing SOX2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Anophthalmia/Microphthalmia, Sequencing SOX2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
367291
  • C Sequence analysis of the entire coding region

Anophthalmia/Microphthalmia/Coloboma/Anterior Segment Dysgenesis

Asper Biogene Asper Biogene LLC
Estonia
3735
  • C Sequence analysis of the entire coding region

Septo-optic dysplasia

Molecular Vision Laboratory
United States
124
  • C Sequence analysis of the entire coding region

Syndromic microphthalmia type 3

Bioarray
Spain
11
  • D Deletion/duplication analysis

Developmental Eye Disease panel

Molecular Vision Laboratory
United States
10759
  • C Sequence analysis of the entire coding region

SOX2

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

Male Factor Infertility

Asper Biogene Asper Biogene LLC
Estonia
9990
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 61 to 80 of 88

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.