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Results: 61 to 80 of 84

Tests names and labsConditionsGenes, analytes, and microbesMethods

Oxidative Phosphorylation Disorders NGS Panel

Fulgent Genetics
United States
416235
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Navajo neurohepatopathy: gene deletion/duplication

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

Mitochondrial DNA Depletion Syndrome , Panel Massive Sequencing (NGS) 14 Genes

Reference Laboratory Genetics
Spain
1714
  • C Sequence analysis of the entire coding region

Mitochondrial Depletion NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3223
  • C Sequence analysis of the entire coding region

MITOCHONDRIAL DNA DEPLETION SYNDROME, HEPATOCEREBRAL FORM

Laboratorio de Genetica Clinica SL
Spain
54
  • C Sequence analysis of the entire coding region

Mitochondrial DNA Depletion Syndrome Type 6 (Hepatocerebral Type) , Sequencing MPV17 Gene

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

Mitochondrial DNA Depletion Syndrome Panel

Blueprint Genetics
Finland
1025
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Navajo neurohepatopathy

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

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37302
  • C Sequence analysis of the entire coding region

MPV17 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

MPV17 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MPV17 Single Gene

Fulgent Genetics
United States
11
  • 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

MPV17 DNA Sequencing Test (Related to mtDNA depletion)

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Mitochondrial Hepatoencephalopathic Evaluation (POLG, DGUOK, MPV17, TWINKLE)

Athena Diagnostics
United States
94
  • C Sequence analysis of the entire coding region

Cholestasis NGS Panel

Fulgent Genetics
United States
12166
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 80 of 84

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.