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Variant : CV534423 (NC_000023.10:g.(?_32235013)_(32716135_?)del) Homo sapiens

Symbol: CV534423
Name: NC_000023.10:g.(?_32235013)_(32716135_?)del
Condition: Duchenne muscular dystrophy [RCV000630668]
Clinical Significance: pathogenic
Last Evaluated: 10/25/2017
Review Status: criteria provided, single submitter
Related Genes: DMD   MIR3915   MIR548F5  
Variant Type: deletion (SO:0000159)
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.(?_32235013)_(32716135_?)del
Human AssemblyChrPosition (strand)Source
GRCh38X32,216,896 - 32,698,018CLINVAR
GRCh37X32,235,013 - 32,716,135CLINVAR
Cytogenetic MapXXp21.1CLINVAR

Disease Annotations
References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13612249
Created: 2018-06-12
Species: Homo sapiens
Last Modified: 2020-03-17
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.