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Variant : CV165199 (GRCh38/hg38 8p23.3(chr8:208048-1576545)x3) Homo sapiens

Symbol: CV165199
Name: GRCh38/hg38 8p23.3(chr8:208048-1576545)x3
Condition: See cases [RCV000143512]
Clinical Significance: uncertain significance
Last Evaluated: 07/16/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC100797.4   AF067845.2   DLGAP2   DLGAP2-AS1   ERICH1   FAM87A   FBXO25   LOC105377777   TDRP   ZNF596  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_208048)_(1576545_?)dup
Human AssemblyChrPosition (strand)Source
GRCh388208,048 - 1,576,545CLINVAR
GRCh378158,048 - 1,524,711CLINVAR
Build 368148,048 - 1,512,118CLINVAR
Cytogenetic Map88p23.3CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9491110
Created: 2014-09-09
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.