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Variant : CV165179 (GRCh38/hg38 12q21.31-21.32(chr12:85722164-86332192)x3) Homo sapiens

Symbol: CV165179
Name: GRCh38/hg38 12q21.31-21.32(chr12:85722164-86332192)x3
Condition: See cases [RCV000143492]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 08/22/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MGAT4C   NTS   RASSF9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000012.12:g.(?_85722164)_(86332192_?)dup
NC_000012.11:g.(?_86115942)_(86725970_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381285,722,164 - 86,332,192CLINVAR
GRCh371286,115,942 - 86,725,970CLINVAR
Build 361284,640,073 - 85,250,101CLINVAR
Cytogenetic Map1212q21.31-21.32CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9491090
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.