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Variant : CV605933 (GRCh37/hg19 15q13.2-13.3(chr15:30394266-32862087)x3) Homo sapiens

Symbol: CV605933
Name: GRCh37/hg19 15q13.2-13.3(chr15:30394266-32862087)x3
Condition: not provided [RCV000751233]
Clinical Significance: pathogenic
Last Evaluated: 10/14/2011
Review Status: no assertion criteria provided
Related Genes: ARHGAP11B   CHRFAM7A   CHRNA7   FAN1   GOLGA8H   GOLGA8O   KLF13   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371530,394,266 - 32,862,087CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366559
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-08-06
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.