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Variant : CV382882 (GRCh37/hg19 8q24.3(chr8:144725942-145508436)x3) Homo sapiens

Symbol: CV382882
Name: GRCh37/hg19 8q24.3(chr8:144725942-145508436)x3
Condition: See cases [RCV000447256]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: BOP1   CCDC166   CYC1   EPPK1   EXOSC4   FAM83H   GPAA1   GRINA   HGH1   MAF1   MAPK15   MIR661   MROH1   NRBP2   OPLAH   PARP10   PLEC   PUF60   SCRIB   SCX   SHARPIN   SPATC1   ZNF623   ZNF707  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh378144,725,942 - 145,508,436CLINVAR
Cytogenetic Map88q24.3CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 12851973
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


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