Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV381253 (GRCh37/hg19 11q22.2(chr11:102323664-102401448)x3) Homo sapiens

Symbol: CV381253
Name: GRCh37/hg19 11q22.2(chr11:102323664-102401448)x3
Condition: See cases [RCV000446744]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: MMP7   TMEM123  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3711102,323,664 - 102,401,448CLINVAR
Cytogenetic Map1111q22.2CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 12851467
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-10-15
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.