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Variant : CV595162 (GRCh37/hg19 2p16.1(chr2:56170392-56636529)x3) Homo sapiens

Symbol: CV595162
Name: GRCh37/hg19 2p16.1(chr2:56170392-56636529)x3
Condition: not provided [RCV000740462]
Clinical Significance: benign
Last Evaluated: 10/06/2015
Review Status: no assertion criteria provided
Related Genes: CCDC85A   MIR216A   MIR217  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37256,170,392 - 56,636,529CLINVAR
Cytogenetic Map22p16.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14355836
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-06-30
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.