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Results: 1 to 20 of 85

Tests names and labsConditionsGenes and analytesMethods

Porphyria variegata

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SGCG Gene Sequencing

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
11
  • C Sequence analysis of the entire coding region

MyoGene Panel (43 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
9543
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophy (LGMD/EDMD) Panel (25 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
6425
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb-girdle muscular dystrophy, autosomal recessive type 2C

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Gamma-Sarcoglycanopathy

(AC) Atlanta Center: Medical Neurogenetics, LLC.
United States
11
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

SGCG. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy (LGMD) NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
2324
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Autosomal Recessive Limb-Girdle Muscular Dystrophy (LGMD) Sequencing Panel

PreventionGenetics
United States
1718
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Limb Girdle Muscular Dystrophy, Type 2C (LGMD2C) via the SGCG Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

LIMB-GIRDLE MUSCULAR DYSTROPHY, A.R.

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2318
  • C Sequence analysis of the entire coding region

LIMB-GIRDLE MUSCULAR DYSTROPHY

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2722
  • C Sequence analysis of the entire coding region

SGCG

MVZ Dortmund Dr. Eberhard and Partner
Germany
11
  • C Sequence analysis of the entire coding region

CarrierMap

Recombine
United States
299297
  • T Targeted variant analysis

Autosomal recessive limb-girdle muscular dystrophy type 2C

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

Limb-girdle muscular dystrophy (deletions/duplications of SGCA, SGCB, SGCD, SGCG and FKRP genes)

CGC Genetics
Portugal
55
  • D Deletion/duplication analysis

Limb-girdle muscular dystrophy type 2C (LGMD2C, sequence analysis of SGCG gene)

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

Limb-girdle muscular dystrophies (NGS panel for 26 genes)

CGC Genetics
Portugal
2626
  • C Sequence analysis of the entire coding region

Sarcoglycanopathies (NGS panel for 5 genes)

CGC Genetics
Portugal
55
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 85

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.