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Variant : CV556178 (GRCh37/hg19 22q12.2(chr22:30902886-31260395)x3) Homo sapiens

Symbol: CV556178
Name: GRCh37/hg19 22q12.2(chr22:30902886-31260395)x3
Condition: not provided [RCV000684469]
Clinical Significance: uncertain significance
Last Evaluated: 01/30/2018
Review Status: no assertion criteria provided
Related Genes: DUSP18   GAL3ST1   OSBP2   PES1   SEC14L6   SLC35E4   TCN2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372230,902,886 - 31,260,395CLINVAR
Cytogenetic Map2222q12.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798705
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-09-08
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.