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Variant : CV604996 (GRCh37/hg19 12p13.2(chr12:12021657-12026937)x0) Homo sapiens

Symbol: CV604996
Name: GRCh37/hg19 12p13.2(chr12:12021657-12026937)x0
Condition: not provided [RCV000750296]
Clinical Significance: benign
Last Evaluated: 03/12/2012
Review Status: no assertion criteria provided
Related Genes: ETV6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371212,021,657 - 12,026,937CLINVAR
Cytogenetic Map1212p13.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14365622
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.