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Results: 1 to 20 of 366

Tests names and labsConditionsGenes, analytes, and microbesMethods

FLNA Gene Otopaladigital syndrome type 1 NGS Genetic DNA Test

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

FLNA Gene Otopaladigital syndrome type 2 NGS Genetic DNA Test

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

FLNA Gene Terminal osseous dysplasis NGS Genetic DNA Test

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

FLNA Gene Cardiac valvular dysplesia, X-linked NGS Genetic DNA Test

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

FLNA Gene Frontometaphyseal dysplasia NGS Genetic DNA Test

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

FLNA Gene Intestinal pseudoobstraction, neuronal NGS Genetic DNA Test

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

FLNA Gene Melnick-Needles syndrome NGS Genetic DNA Test

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

FLNA Gene Heterotopia, periventricular, ED variant NGS Genetic DNA Test

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

FLNA Gene Heterotopia, periventricular, X-linked dominant NGS Genetic DNA Test

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

FLNA Gene FG syndrome type 2 NGS Genetic DNA Test

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

Comprehensive Aortopathy Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
5448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ehlers-Danlos Syndrome Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
2822
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marfan and Related Conditions Panel

Mayo Clinic Laboratories Mayo Clinic
United States
3730
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region

Comprehensive Epilepsy Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1318
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

PlateletGenex Thrombocytopenia Panel (26 genes) (2 Day STAT TAT)

Machaon Diagnostics
United States
2226
  • C Sequence analysis of the entire coding region

Aortic diseases Panel

Health in Code
Spain
7135
  • C Sequence analysis of the entire coding region

Congenital heart diseases Panel

Health in Code
Spain
176
  • C Sequence analysis of the entire coding region

Cardiovascular Diseases_General Panel

Health in Code
Spain
1380
  • C Sequence analysis of the entire coding region

Congenital Heart Diseases Panel

Health in Code
Spain
139
  • C Sequence analysis of the entire coding region

Cardiomyopathies Panel

Health in Code
Spain
1149
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 366

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.