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Variant : CV160300 (GRCh38/hg38 12p13.31(chr12:9244854-9541356)x3) Homo sapiens

Symbol: CV160300
Name: GRCh38/hg38 12p13.31(chr12:9244854-9541356)x3
Condition: See cases [RCV000139389]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00987   LINC02367  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000012.12:g.(?_9244854)_(9541356_?)dup
NC_000012.11:g.(?_9397450)_(9693952_?)dup
NC_000012.10:g.(?_9288717)_(9585219_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38129,244,854 - 9,541,356CLINVAR
GRCh37129,397,450 - 9,693,952CLINVAR
Build 36129,288,717 - 9,585,219CLINVAR
Cytogenetic Map1212p13.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486920
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.