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Variant : CV653368 (NC_000023.10:g.(?_32490271)_(32669194_?)del) Homo sapiens

Symbol: CV653368
Name: NC_000023.10:g.(?_32490271)_(32669194_?)del
Condition: Duchenne muscular dystrophy [RCV000794828]
Clinical Significance: pathogenic
Last Evaluated: 10/24/2018
Review Status: criteria provided, single submitter
Related Genes: DMD   MIR3915   MIR548F5  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.(?_32490271)_(32669194_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X32,472,154 - 32,651,077CLINVAR
GRCh37X32,490,271 - 32,669,194CLINVAR
Cytogenetic MapXXp21.1CLINVAR



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14714011
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE



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