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Variant : CV435616 (GRCh37/hg19 8q24.3(chr8:144779442-146113113)x3) Homo sapiens

Symbol: CV435616
Name: GRCh37/hg19 8q24.3(chr8:144779442-146113113)x3
Condition: See cases [RCV000510396]
Clinical Significance: uncertain significance
Last Evaluated: 08/01/2014
Review Status: no assertion criteria provided
Related Genes: ADCK5   ARHGAP39   BOP1   C8orf82   CCDC166   COMMD5   CPSF1   CYC1   CYHR1   DGAT1   EPPK1   EXOSC4   FAM83H   FBXL6   FOXH1   GPAA1   GPT   GRINA   HGH1   HSF1   KIFC2   LRRC14   LRRC24   MAF1   MAPK15   MFSD3   MIR1234   MIR661   MROH1   NRBP2   OPLAH   PARP10   PLEC   PPP1R16A   PUF60   RECQL4   RPL8   SCRIB   SCRT1   SCX   SHARPIN   SLC39A4   SLC52A2   SPATC1   TMEM249   TONSL   VPS28   ZNF250   ZNF251   ZNF34   ZNF517   ZNF7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378144,779,442 - 146,113,113CLINVAR
Cytogenetic Map88q24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443375
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
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.