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Variant : CV472026 (NC_000023.10:g.(?_32429849)_(32632590_?)del) Homo sapiens

Symbol: CV472026
Name: NC_000023.10:g.(?_32429849)_(32632590_?)del
Condition: Duchenne muscular dystrophy [RCV000558895]
Clinical Significance: pathogenic
Last Evaluated: 01/13/2017
Review Status: criteria provided, single submitter
Related Genes: DMD   MIR3915  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.(?_32429849)_(32632590_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X32,411,732 - 32,614,473CLINVAR
GRCh37X32,429,849 - 32,632,590CLINVAR
Cytogenetic MapXXp21.1CLINVAR



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13494419
Created: 2018-01-09
Species: Homo sapiens
Last Modified: 2020-03-17
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.