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Variant : CV471174 (NC_000023.10:g.(?_31893285)_(33357402_?)del) Homo sapiens

Symbol: CV471174
Name: NC_000023.10:g.(?_31893285)_(33357402_?)del
Condition: Duchenne muscular dystrophy [RCV000528858]
Clinical Significance: pathogenic
Last Evaluated: 08/07/2017
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.(?_31893285)_(33357402_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X31,875,168 - 33,339,285CLINVAR
GRCh37X31,893,285 - 33,357,402CLINVAR
Cytogenetic MapXXp21.1CLINVAR
Trait Synonyms: Muscular dystrophy, pseudohypertrophic progressive, Duchenne type



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13481178
Created: 2018-01-09
Species: Homo sapiens
Last Modified: 2020-05-19
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.