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Variant : CV596579 (GRCh37/hg19 22q11.23(chr22:25169549-25303941)x3) Homo sapiens

Symbol: CV596579
Name: GRCh37/hg19 22q11.23(chr22:25169549-25303941)x3
Condition: not provided [RCV000741879]
Clinical Significance: benign
Last Evaluated: 11/05/2013
Review Status: no assertion criteria provided
Related Genes: PIWIL3   SGSM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372225,169,549 - 25,303,941CLINVAR
Cytogenetic Map2222q11.23CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14357253
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-29
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.