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Results: 61 to 76 of 76

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

Hereditary Optic Atrophy

MGZ Medical Genetics Center
Germany
37
  • C Sequence analysis of the entire coding region

Opticus atrophy 1

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • D Deletion/duplication analysis

OPA1 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

mtDNA Depletion Syndrome NGS Panel

Fulgent Genetics
United States
8616
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Optic Atrophy Evaluation (OPA1)

Athena Diagnostics
United States
21
  • C Sequence analysis of the entire coding region

OPA1 DNA Sequencing Test (Related to mtDNA depletion)

Athena Diagnostics
United States
21
  • C Sequence analysis of the entire coding region

OPA1 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myopathy-Rhabdomyolysis NGS Panel

Fulgent Genetics
United States
3729
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glaucoma NGS Panel

Fulgent Genetics
United States
6826
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Optic Atrophy Type 1

MGZ Medical Genetics Center
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Optic Atrophy Type 1 and Deafness

MGZ Medical Genetics Center
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Optic atrophy type 1

Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet
Denmark
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 61 to 76 of 76

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.