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Variant : CV435400 (GRCh37/hg19 2q37.3(chr2:241315690-241645335)x3) Homo sapiens

Symbol: CV435400
Name: GRCh37/hg19 2q37.3(chr2:241315690-241645335)x3
Condition: See cases [RCV000511888]
Clinical Significance: uncertain significance
Last Evaluated: 08/22/2014
Review Status: no assertion criteria provided
Related Genes: ANKMY1   AQP12A   AQP12B   CAPN10   DUSP28   GPC1   GPR35   MIR149   RNPEPL1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372241,315,690 - 241,645,335CLINVAR
Cytogenetic Map22q37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444857
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.