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Variant : CV596741 (GRCh37/hg19 22q13.31(chr22:46484973-46535894)x1) Homo sapiens

Symbol: CV596741
Name: GRCh37/hg19 22q13.31(chr22:46484973-46535894)x1
Condition: not provided [RCV000742041]
Clinical Significance: benign
Last Evaluated: 11/27/2011
Review Status: no assertion criteria provided
Related Genes: MIRLET7A3   MIRLET7B  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh372246,484,973 - 46,535,894CLINVAR
Cytogenetic Map2222q13.31CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14357415
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-22
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.