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Variant : CV384170 (GRCh37/hg19 22q12.2(chr22:30021252-30305283)x3) Homo sapiens

Symbol: CV384170
Name: GRCh37/hg19 22q12.2(chr22:30021252-30305283)x3
Condition: See cases [RCV000447326]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ASCC2   CABP7   MTMR3   NF2   UQCR10   ZMAT5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372230,021,252 - 30,305,283CLINVAR
Cytogenetic Map2222q12.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12852043
Created: 2017-04-11
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.