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Variant : CV596424 (GRCh37/hg19 22q11.21(chr22:18650746-19743640)x1) Homo sapiens

Symbol: CV596424
Name: GRCh37/hg19 22q11.21(chr22:18650746-19743640)x1
Condition: not provided [RCV000741724]
Clinical Significance: benign
Last Evaluated: 03/13/2013
Review Status: no assertion criteria provided
Related Genes: C22orf39   CDC45   CLDN5   CLTCL1   DGCR2   DGCR6   ESS2   GP1BB   GSC2   HIRA   MRPL40   PRODH   SEPTIN5   SLC25A1   TSSK2   UFD1   USP18  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372218,650,746 - 19,743,640CLINVAR
Cytogenetic Map2222q11.21CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14357098
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-08-04
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.