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Variant : CV162683 (GRCh38/hg38 12p13.31(chr12:8839030-9134304)x3) Homo sapiens

Symbol: CV162683
Name: GRCh38/hg38 12p13.31(chr12:8839030-9134304)x3
Condition: See cases [RCV000141433]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: A2M   A2M-AS1   A2ML1   KLRG1   LINC00612   M6PR   PHC1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000012.12:g.(?_8839030)_(9134304_?)dup
NC_000012.11:g.(?_8991626)_(9286900_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38128,839,030 - 9,134,304CLINVAR
GRCh37128,991,626 - 9,286,900CLINVAR
Build 36128,882,893 - 9,178,167CLINVAR
Cytogenetic Map1212p13.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488958
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.