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Variant : CV592477 (GRCh37/hg19 12p13.2(chr12:11411923-11912896)x3) Homo sapiens

Symbol: CV592477
Name: GRCh37/hg19 12p13.2(chr12:11411923-11912896)x3
Condition: not provided [RCV000737777]
Clinical Significance: benign
Last Evaluated: 03/23/2011
Review Status: no assertion criteria provided
Related Genes: ETV6   PRB1   PRB2   PRB3   PRB4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371211,411,923 - 11,912,896CLINVAR
Cytogenetic Map1212p13.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353144
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-05
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.