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Variant : CV534920 (NC_000023.10:g.(?_32456338)_(32841967_?)dup) Homo sapiens

Symbol: CV534920
Name: NC_000023.10:g.(?_32456338)_(32841967_?)dup
Condition: Duchenne muscular dystrophy [RCV000630656]
Clinical Significance: uncertain significance
Last Evaluated: 12/19/2017
Review Status: criteria provided, single submitter
Related Genes: DMD   MIR3915   MIR548F5  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.(?_32456338)_(32841967_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X32,438,221 - 32,823,850CLINVAR
GRCh37X32,456,338 - 32,841,967CLINVAR
Cytogenetic MapXXp21.1CLINVAR



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13612213
Created: 2018-06-12
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.