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Results: 1 to 20 of 246

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cardiomyopathy, dilated, 1C, with or without LVNC, 601493, Autosomal dominant; CMD1C (Familial isolated dilated cardiomyopathy) (LDB3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Cardiomyopathy, hypertrophic, 24, 601493, Autosomal dominant (LDB3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Left ventricular noncompaction 3, 601493, Autosomal dominant (Left ventricular noncompaction) (LDB3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
88134
  • X Mutation scanning of select exons

Cardiology Sequencing- Full Panel (174 Genes)

Genesys Diagnostics Genesys Diagnostics, Inc.
United States
122174
  • X Mutation scanning of select exons

LDB3 Gene Cardiomyopathy, dilated type 1C NGS Genetic DNA Test

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

LDB3 Gene Myopathy, myofibrillar, ZASP related NGS Genetic DNA Test

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

LDB3 Gene Cardiomyopathy, hypertrophic, type 24 NGS Genetic DNA Test

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

Distal Weakness Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1216
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular Disorders exome

Genetic Services Laboratory University of Chicago
United States
116137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophy Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
175
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathies General Panel

Health in Code
Spain
1173
  • C Sequence analysis of the entire coding region

Hypertrophic cardiomyopathy extended panel

Health in Code
Spain
1104
  • C Sequence analysis of the entire coding region

Arrhythmia General Panel

Health in Code
Spain
1218
  • C Sequence analysis of the entire coding region

Cardiac conduction disease Panel

Health in Code
Spain
134
  • C Sequence analysis of the entire coding region

Skeletal myopathy Panel

Health in Code
Spain
157
  • C Sequence analysis of the entire coding region

Non-compaction cardiomyopathy

Health in Code
Spain
137
  • 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

Ventricular arrhythmia and sudden death without structural heart disease

Health in Code
Spain
177
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 246

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.