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Variant : CV602101 (GRCh37/hg19 8p23.1(chr8:11928524-12534362)x3) Homo sapiens

Symbol: CV602101
Name: GRCh37/hg19 8p23.1(chr8:11928524-12534362)x3
Condition: not provided [RCV000747401]
Clinical Significance: benign
Last Evaluated: 09/27/2012
Review Status: no assertion criteria provided
Related Genes: DEFB130A   FAM86B1   FAM86B2   USP17L2   USP17L7   ZNF705D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37811,928,524 - 12,534,362CLINVAR
Cytogenetic Map88p23.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14362746
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-06-30
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.