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Variant : CV623779 (NC_000023.10:g.85296959_85303375inv) Homo sapiens

Symbol: CV623779
Name: NC_000023.10:g.85296959_85303375inv
Condition: Choroideremia [RCV000787471]
Clinical Significance: pathogenic
Last Evaluated: 04/09/2019
Review Status: no assertion criteria provided
Related Genes: CHM  
Variant Type: inversion (SO:1000036)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.85296959_85303375inv
Position
Human AssemblyChrPosition (strand)Source
GRCh37X85,296,959 - 85,303,375CLINVAR
Cytogenetic MapXXq21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14698914
Created: 2019-08-06
Species: Homo sapiens
Last Modified: 2019-09-10
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.