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Variant : CV597026 (GRCh37/hg19 3p24.2(chr3:25564929-25654677)x3) Homo sapiens

Symbol: CV597026
Name: GRCh37/hg19 3p24.2(chr3:25564929-25654677)x3
Condition: not provided [RCV000742326]
Clinical Significance: benign
Last Evaluated: 12/16/2016
Review Status: no assertion criteria provided
Related Genes: RARB   TOP2B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37325,564,929 - 25,654,677CLINVAR
Cytogenetic Map33p24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14357698
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-19
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.