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Unknown type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (6):

Duchenne muscular dystrophy; Becker muscular dystrophy; Caveolinopathies more...

Genes (12):

BAG3 (10q26.11); CRYAB (11q23.1); DES (2q35); FHL1 (Xq26.3); FLNC (7q32.1) more...

Conditions

Total conditions: 6

Condition/Phenotype	Identifier

Methodology

Total methods: 0

Method Category

Test method

Instrument *

* Instrument: Not provided

Technical Information

Recommended fields not provided:

Test Confirmation

Additional Information

Reviews:

PubMed Clinical Queries

Reviews in PubMed

Clinical resources:

Clinicaltrials.gov

Molecular resources:

View DMD variations in ClinVar

Coriell Institute for Medical Research

Practice guidelines:

ACMG Algorithm, 2022

Consumer resources:

Genetic Alliance

MedlinePlusGenetics (GHR)

NCATS Office of Rare Diseases Research (GARD)

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in 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.