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Variant : CV555355 (GRCh37/hg19 15q13.1-13.2(chr15:28968634-31073669)x3) Homo sapiens

Symbol: CV555355
Name: GRCh37/hg19 15q13.1-13.2(chr15:28968634-31073669)x3
Condition: not provided [RCV000683660]
Clinical Significance: uncertain significance
Last Evaluated: 08/23/2017
Review Status: no assertion criteria provided
Related Genes: APBA2   ARHGAP11B   CHRFAM7A   FAM189A1   GOLGA8H   GOLGA8J   GOLGA8M   NSMCE3   TJP1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371528,968,634 - 31,073,669CLINVAR
Cytogenetic Map1515q13.1-13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13797316
Created: 2018-10-09
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.