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Variant : CV553811 (GRCh37/hg19 2q31.2(chr2:178546905-179656720)x3) Homo sapiens

Symbol: CV553811
Name: GRCh37/hg19 2q31.2(chr2:178546905-179656720)x3
Condition: not provided [RCV000682116]
Clinical Significance: uncertain significance
Last Evaluated: 04/26/2018
Review Status: no assertion criteria provided
Related Genes: FKBP7   OSBPL6   PDE11A   PJVK   PLEKHA3   PRKRA   RBM45   TTN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372178,546,905 - 179,656,720CLINVAR
Cytogenetic Map22q31.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13794882
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-03-17
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.