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Variant : CV382141 (GRCh37/hg19 11q22.2(chr11:102249285-102323664)x3) Homo sapiens

Symbol: CV382141
Name: GRCh37/hg19 11q22.2(chr11:102249285-102323664)x3
Condition: See cases [RCV000447841]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: BIRC2   TMEM123  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711102,249,285 - 102,323,664CLINVAR
Cytogenetic Map1111q22.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12852554
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-10-08
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.