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Variant : CV592355 (GRCh37/hg19 11q22.2(chr11:102300876-102306750)x1) Homo sapiens

Symbol: CV592355
Name: GRCh37/hg19 11q22.2(chr11:102300876-102306750)x1
Condition: not provided [RCV000737655]
Clinical Significance: benign
Last Evaluated: 02/08/2013
Review Status: no assertion criteria provided
Related Genes: TMEM123  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711102,300,876 - 102,306,750CLINVAR
Cytogenetic Map1111q22.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14353022
Created: 2019-02-12
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.