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Variant : CV674706 (GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3) Homo sapiens

Symbol: CV674706
Name: GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3
Condition: not provided [RCV000847820]
Clinical Significance: pathogenic
Last Evaluated: 05/31/2017
Review Status: no assertion criteria provided
Related Genes: ABLIM1   ABRAXAS2   ACADSB   ADAM12   ADAM8   ADGRA1   ADRB1   AFAP1L2   ARMS2   ATE1   ATRNL1   BAG3   BCCIP   BNIP3   BTBD16   BUB3   C10orf120   C10orf82   C10orf88   C10orf90   CACUL1   CALY   CASC2   CASP7   CCDC172   CCDC186   CFAP46   CHST15   CLRN3   CPXM2   CTBP2   CUZD1   CYP2E1   DCLRE1A   DENND10   DHX32   DMBT1   DOCK1   DPYSL4   EBF3   ECHS1   EDRF1   EEF1AKMT2   EIF3A   EMX2   EMX2OS   ENO4   FAM160B1   FAM204A   FAM24A   FAM24B   FAM53B   FANK1   FGFR2   FOXI2   FUOM   GFRA1   GLRX3   GPR26   GRK5   HABP2   HMX2   HMX3   HSPA12A   HTRA1   IKZF5   INPP5A   INPP5F   INSYN2A   JAKMIP3   KCNK18   KNDC1   LHPP   LINC01166   LINC02870   LRRC27   MCMBP   MGMT   MKI67   MMP21   MTG1   NANOS1   NHLRC2   NKX1-2   NKX6-2   NPS   NRAP   NSMCE4A   OAT   PAOX   PDZD8   PLEKHA1   PLEKHS1   PLPP4   PNLIP   PNLIPRP1   PNLIPRP2   PNLIPRP3   PPP2R2D   PRAP1   PRDX3   PRLHR   PSTK   PTPRE   PWWP2B   RAB11FIP2   RGS10   SEC23IP   SFXN4   SHTN1   SLC18A2   SPRN   STK32C   SYCE1   TACC2   TCERG1L   TCERG1L-AS1   TCF7L2   TDRD1   TEX36   TIAL1   TRUB1   TUBGCP2   UROS   UTF1   VAX1   VENTX   VTI1A   VWA2   WDR11   ZNF511   ZRANB1  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3710114,544,537 - 135,427,143CLINVAR
Cytogenetic Map1010q25.2-26.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14975322
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-05-26
Status: ACTIVE


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