U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 1 to 20 of 25

Tests names and labsConditionsGenes, analytes, and microbesMethods

SPAST Gene SPG4 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

CPT1B Gene Carnitine palmitoyltransferase 1B deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

CPT1B - Carnitine Palmitoyltransferase deficiency type Ib

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Fatty Acid Oxidation Panel (MitomeNGS)

Baylor Genetics
United States
1617
  • C Sequence analysis of the entire coding region

Myopathies, including congenital myopathies (WES based NGS panel of 180 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
1180
  • C Sequence analysis of the entire coding region

Rhabdomyolysis and metabolic muscle diseases (WES based NGS panel of 55 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
155
  • C Sequence analysis of the entire coding region

Carnitine palmitoyltransferase I deficiency (deletion/duplication analysis on CPT1B gene)

CGC Genetics Unilabs
Portugal
11
  • D Deletion/duplication analysis

Carnitine palmitoyltransferase IB deficiency (sequence analysis of CPT1B gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

MUSCULAR DISORDERS- EMCG GLOBAL EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1416
  • E Sequence analysis of select exons

MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES)

Laboratorio de Genetica Clinica SL
Spain
11372
  • E Sequence analysis of select exons

CPT1B Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

CPT1B Comprehensive - Sequence & Deletion/Duplication Analysis

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

CPT1B Deletion/Duplication Analysis

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

CPT1B Sequence Analysis

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

CPT1B Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

Autism/ID Xpanded Panel

GeneDx
United States
22592
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NewbornDx Advanced Sequencing Evaluation

Athena Diagnostics
United States
11722
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lipid Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
8071
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fatty Acid Oxidation Deficiency

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
422
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 25

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.