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Variant : CV602098 (GRCh37/hg19 8p23.1(chr8:11648789-11898209)x3) Homo sapiens

Symbol: CV602098
Name: GRCh37/hg19 8p23.1(chr8:11648789-11898209)x3
Condition: not provided [RCV000747398]
Clinical Significance: benign
Last Evaluated: 03/11/2013
Review Status: no assertion criteria provided
Related Genes: CTSB   DEFB134   DEFB135   DEFB136   FDFT1  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37811,648,789 - 11,898,209CLINVAR
Cytogenetic Map88p23.1CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14362743
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-06-30
Status: ACTIVE


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