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Variant : CV675723 (GRCh37/hg19 8p12-11.1(chr8:36094421-43822214)x3) Homo sapiens

Symbol: CV675723
Name: GRCh37/hg19 8p12-11.1(chr8:36094421-43822214)x3
Condition: not provided [RCV000848822]
Clinical Significance: uncertain significance
Last Evaluated: 09/17/2018
Review Status: no assertion criteria provided
Related Genes: ADAM18   ADAM2   ADAM32   ADAM9   ADGRA2   ADRB3   ANK1   AP3M2   ASH2L   BAG4   BRF2   C8orf86   CHRNA6   CHRNB3   DDHD2   DKK4   EIF4EBP1   ERLIN2   FGFR1   FNTA   GINS4   GOLGA7   GOT1L1   GPAT4   HGSNAT   HOOK3   HTRA4   IDO1   IDO2   IKBKB   KAT6A   KCNU1   LETM2   LSM1   NKX6-3   NSD3   PLAT   PLEKHA2   PLPBP   PLPP5   POLB   POMK   POTEA   RAB11FIP1   RNF170   SFRP1   SLC20A2   SMIM19   STAR   TACC1   TCIM   THAP1   TM2D2   VDAC3   ZMAT4   ZNF703  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37836,094,421 - 43,822,214CLINVAR
Cytogenetic Map88p12-11.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14975331
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-31
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.