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Variant : CV804772 (GRCh37/hg19 22q13.2(chr22:41871935-42026428)x1) Homo sapiens

Symbol: CV804772
Name: GRCh37/hg19 22q13.2(chr22:41871935-42026428)x1
Condition: not provided [RCV001007503]
Clinical Significance: uncertain significance
Last Evaluated: 05/14/2019
Review Status: no assertion criteria provided
Related Genes: ACO2   CSDC2   DESI1   PMM1   POLR3H   XRCC6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372241,871,935 - 42,026,428CLINVAR
Cytogenetic Map2222q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25317443
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-09-08
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.