Clinical and research tests for 607137 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 49

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Comprehensive Neuromuscular Panel PreventionGenetics, part of Exact Sciences United States	183	142	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Comprehensive Muscular Dystrophy Panel Labcorp Genetics (formerly Invitae) LabCorp United States	114	52	D Deletion/duplication analysis
Invitae Limb-Girdle Muscular Dystrophy Panel Labcorp Genetics (formerly Invitae) LabCorp United States	91	37	D Deletion/duplication analysis
Invitae Comprehensive Neuromuscular Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States	353	208	D Deletion/duplication analysis
Limb Girdle Muscular Dystrophy (LGMD) Panel PreventionGenetics, part of Exact Sciences United States	34	35	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
GeneSeq® Neuro: Limb-Girdle and Emery-Dreifuss Muscular Dystrophies MNG Laboratories (Medical Neurogenetics, LLC.) United States	2	43	C Sequence analysis of the entire coding region
Neuromuscular Disorders Panel Baylor Genetics United States	1	142	C Sequence analysis of the entire coding region
Neuromuscular diseases panel_v.2.0 CGC Genetics Unilabs Portugal	17	248	C Sequence analysis of the entire coding region
Limb-girdle muscular dystrophy type 1G (LGMD1G, sequence analysis of HNRNPDL gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Neuromuscular Diseases Panel (Expanded) Mendelics Brazil	1	288	C Sequence analysis of the entire coding region
Neuromuscular Diseases Panel (DNAmplo) Mendelics Brazil	1	109	C Sequence analysis of the entire coding region
LIMB-GIRDLE MUSCULAR DYSTROPHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	54	E Sequence analysis of select exons
MUSCULAR DISORDERS- EMCG GLOBAL EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	416	E Sequence analysis of select exons
MUSCULAR DYSTROPHIES/ MYOPATHIES PANEL Laboratorio de Genetica Clinica SL Spain	1	250	E Sequence analysis of select exons
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Xpanded Adult Movement Disorders Panel GeneDx United States	5	473	C Sequence analysis of the entire coding region
Muscular dystrophy, limb-girdle, autosomal dominant: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	5	7	C Sequence analysis of the entire coding region
HNRNPDL Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Limb-Girdle Muscular Dystrophy Asper Biogene Asper Biogene LLC Estonia	87	39	C Sequence analysis of the entire coding region
Limb-Girdle Muscular Dystrophy type 1 Laboratory of Human Genetics GENOMED Health Care Center Poland	1	7	C Sequence analysis of the entire coding region

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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.

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Results: 21 to 40 of 49

Results: 21 to 40 of 49