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Results: 1 to 20 of 32

Tests names and labsConditionsGenes, analytes, and microbesMethods

CNBP Gene Myotonic dystrophy type 2 NGS Genetic DNA Test

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

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

qGenEx Intellectual disability

Quantitative Genomic Medicine Laboratories, SL
Spain
31969
  • S Mutation scanning of the entire coding region
  • 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

MUSCULAR DISORDERS- EMCG GLOBAL EXOME PANEL

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

MI Tumor Seek Hybrid

Caris Life Sciences
United States
1591
  • R RNA analysis
  • C Sequence analysis of the entire coding region

CoGenesis@Neuro

Codex Genetics Limited
Hong Kong
1490
  • T Targeted variant analysis

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Myotonic Dystrophy Type 2

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

Sarcoma Comprehensive NGS Fusion Panel

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
197
  • C Sequence analysis of the entire coding region

Myotonia Panel

GeneDx
United States
1210
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

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

Neuromuscular disorders - different panels

Institute of Human Genetics Cologne University
Germany
16474
  • D Deletion/duplication analysis
  • 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

Caris MI TumorSeek Comprehensive Genomic Profile

Caris Life Sciences
United States
1591
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 32

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.