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Variant : CV593414 (GRCh37/hg19 15q13.2(chr15:30737344-30968006)x1) Homo sapiens

Symbol: CV593414
Name: GRCh37/hg19 15q13.2(chr15:30737344-30968006)x1
Condition: not provided [RCV000738714]
Clinical Significance: benign
Last Evaluated: 05/20/2016
Review Status: no assertion criteria provided
Related Genes: ARHGAP11B   GOLGA8H  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371530,737,344 - 30,968,006CLINVAR
Cytogenetic Map1515q13.2CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14354094
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-01
Status: ACTIVE


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