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Variant : CV556192 (GRCh37/hg19 22q13.2-13.31(chr22:44023172-44744568)x3) Homo sapiens

Symbol: CV556192
Name: GRCh37/hg19 22q13.2-13.31(chr22:44023172-44744568)x3
Condition: not provided [RCV000684483]
Clinical Significance: uncertain significance
Last Evaluated: 01/03/2018
Review Status: no assertion criteria provided
Related Genes: EFCAB6   PARVB   PARVG   PNPLA3   PNPLA5   SAMM50   SHISAL1   SULT4A1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372244,023,172 - 44,744,568CLINVAR
Cytogenetic Map2222q13.2-13.31CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798719
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.