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Variant : CV605929 (GRCh37/hg19 15q13.2(chr15:30361587-31089526)x3) Homo sapiens

Symbol: CV605929
Name: GRCh37/hg19 15q13.2(chr15:30361587-31089526)x3
Condition: not provided [RCV000751229]
Clinical Significance: benign
Last Evaluated: 12/22/2016
Review Status: no assertion criteria provided
Related Genes: ARHGAP11B   CHRFAM7A   GOLGA8H   GOLGA8J  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371530,361,587 - 31,089,526CLINVAR
Cytogenetic Map1515q13.2CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14366555
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-15
Status: ACTIVE


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