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Variant : CV555058 (GRCh37/hg19 11p14.3-14.1(chr11:25090108-28909131)x3) Homo sapiens

Symbol: CV555058
Name: GRCh37/hg19 11p14.3-14.1(chr11:25090108-28909131)x3
Condition: not provided [RCV000683363]
Clinical Significance: uncertain significance
Last Evaluated: 06/08/2017
Review Status: no assertion criteria provided
Related Genes: ANO3   BBOX1   BDNF   BDNF-AS   CCDC34   FIBIN   KIF18A   LGR4   LIN7C   LUZP2   METTL15   MIR610   MUC15   SLC5A12  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371125,090,108 - 28,909,131CLINVAR
Cytogenetic Map1111p14.3-14.1CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 13796514
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-09-22
Status: ACTIVE


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