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Results: 1 to 20 of 22

Tests names and labsConditionsGenes, analytes, and microbesMethods

CNBP - Repeat expansion analysis

Centogene AG - the Rare Disease Company
Germany
11
  • T Targeted variant analysis

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myotonic dystrophy 2, 602668, Autosomal dominant; DM2 (Proximal myotonic myopathy)(Repeat Analysis)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • T Targeted variant analysis

Genomic Unity Neuromuscular Disorders Analysis (includes STR analysis of CNBP, DMPK, GIPC1, LRP12, RFC1 and VWA1 genes).

Variantyx, Inc.
United States
53
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Myotonic dystrophy type 2 (CCTG expansion on CNBP/ZNF9 gene)

CGC Genetics Unilabs
Portugal
11
  • T Targeted variant analysis

Myotonic Dystrophy Type 2

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
11
  • T Targeted variant analysis

Myotonic Dystrophy 2 (ZNF9/CNBP) Genetic Testing (Repeat Expansion)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
11
  • E Sequence analysis of select exons

CNBP Repeat Analysis

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

Myotonic dystrophy: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
22
  • C Sequence analysis of the entire coding region

Myotonic Dystrophy Type 2 (CNBP) Repeat Expansion

Fulgent Genetics
United States
11
  • T Targeted variant analysis

Myotonic dystrophy type 2

CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario
Canada
11
  • T Targeted variant analysis

MYOTONIC DYSTROPHY TYPE 2

Laboratorio de Genetica Clinica SL
Spain
11
  • T Targeted variant analysis

Myotonic Syndrome Advanced Evaluation

Athena Diagnostics
United States
97
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Proximal myotonic myopathy

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

Myotone Dystrophy Type 2

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • E Sequence analysis of select exons

Myotone Dystrophy Type 2

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • E Sequence analysis of select exons

CNBP Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CNBP DNA Test (DM2)

Athena Diagnostics
United States
11
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myotonic dystrophy II

Praxis fuer Humangenetik Wien
Austria
11
  • T Targeted variant analysis

Results: 1 to 20 of 22

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.