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Variant : CV592303 (GRCh37/hg19 11q14.1(chr11:85266321-85545180)x3) Homo sapiens

Symbol: CV592303
Name: GRCh37/hg19 11q14.1(chr11:85266321-85545180)x3
Condition: not provided [RCV000737603]
Clinical Significance: benign
Last Evaluated: 04/09/2013
Review Status: no assertion criteria provided
Related Genes: CCDC89   CREBZF   DLG2   SYTL2   TMEM126A   TMEM126B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371185,266,321 - 85,545,180CLINVAR
Cytogenetic Map1111q14.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352970
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.