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Variant : CV593415 (GRCh37/hg19 15q13.2(chr15:30884660-30949625)x1) Homo sapiens

Symbol: CV593415
Name: GRCh37/hg19 15q13.2(chr15:30884660-30949625)x1
Condition: not provided [RCV000738715]
Clinical Significance: benign
Last Evaluated: 12/15/2011
Review Status: no assertion criteria provided
Related Genes: ARHGAP11B   GOLGA8H  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371530,884,660 - 30,949,625CLINVAR
Cytogenetic Map1515q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14354095
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-08
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.