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Variant : CV554986 (GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3) Homo sapiens

Symbol: CV554986
Name: GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3
Condition: not provided [RCV000683291]
Clinical Significance: pathogenic
Last Evaluated: 07/08/2017
Review Status: no assertion criteria provided
Related Genes: ABCC2   ABLIM1   ABRAXAS2   ACADSB   ACSL5   ACSM6   ACTR1A   ADAM12   ADAM8   ADD3   ADGRA1   ADRA2A   ADRB1   AFAP1L2   ALDH18A1   ANKRD2   ARHGAP19   ARL3   ARMH3   ARMS2   AS3MT   ATE1   ATP5MD   ATRNL1   AVPI1   BAG3   BBIP1   BCCIP   BLNK   BLOC1S2   BNIP3   BORCS7   BTBD16   BTRC   BUB3   C10orf120   C10orf62   C10orf82   C10orf88   C10orf90   C10orf95   CACUL1   CALHM1   CALHM2   CALHM3   CALY   CASC2   CASP7   CC2D2B   CCDC172   CCDC186   CCNJ   CEP55   CFAP43   CFAP46   CFAP58   CHST15   CHUK   CLRN3   CNNM1   CNNM2   COL17A1   COX15   CPN1   CPXM2   CRTAC1   CTBP2   CUEDC2   CUTC   CUZD1   CWF19L1   CYP17A1   CYP26A1   CYP26C1   CYP2C18   CYP2C19   CYP2C8   CYP2C9   CYP2E1   DCLRE1A   DENND10   DHX32   DMBT1   DNMBP   DNTT   DOCK1   DPCD   DPYSL4   DUSP5   EBF3   ECHS1   EDRF1   EEF1AKMT2   EIF3A   ELOVL3   EMX2   EMX2OS   ENO4   ENTPD1   ENTPD7   ERLIN1   EXOC6   EXOSC1   FAM160B1   FAM204A   FAM24A   FAM24B   FAM53B   FANK1   FBXL15   FBXW4   FFAR4   FGF8   FGFR2   FOXI2   FRA10AC1   FRAT1   FRAT2   FUOM   GBF1   GFRA1   GLRX3   GOLGA7B   GOT1   GPAM   GPR26   GRK5   GSTO1   GSTO2   HABP2   HELLS   HHEX   HIF1AN   HMX2   HMX3   HOGA1   HPS1   HPS6   HPSE2   HSPA12A   HTRA1   IKZF5   INA   INPP5A   INPP5F   INSYN2A   ITPRIP   JAKMIP3   KAZALD1   KCNIP2   KCNK18   KIF11   KNDC1   LBX1   LCOR   LDB1   LGI1   LHPP   LINC01166   LINC02870   LOXL4   LRRC27   LZTS2   MARVELD1   MCMBP   MFSD13A   MGMT   MIR146B   MKI67   MMP21   MMS19   MORN4   MRPL43   MTG1   MXI1   MYOF   NANOS1   NDUFB8   NEURL1   NFKB2   NHLRC2   NKX1-2   NKX2-3   NKX6-2   NOC3L   NOLC1   NPM3   NPS   NRAP   NSMCE4A   NT5C2   OAT   OGA   OPALIN   PAOX   PAX2   PCGF6   PDCD11   PDCD4   PDE6C   PDLIM1   PDZD7   PDZD8   PGAM1   PI4K2A   PIK3AP1   PITX3   PKD2L1   PLCE1   PLEKHA1   PLEKHS1   PLPP4   PNLIP   PNLIPRP1   PNLIPRP2   PNLIPRP3   POLL   PPP2R2D   PPRC1   PRAP1   PRDX3   PRLHR   PSD   PSTK   PTPRE   PWWP2B   PYROXD2   R3HCC1L   RAB11FIP2   RBM20   RBP4   RGS10   RRP12   SCD   SEC23IP   SEC31B   SEMA4G   SFR1   SFRP5   SFXN2   SFXN3   SFXN4   SH3PXD2A   SHOC2   SHTN1   SLC18A2   SLC25A28   SLC35G1   SLF2   SLIT1   SLK   SMC3   SMNDC1   SNORA12   SORBS1   SORCS1   SORCS3   SPRN   STK32C   STN1   SUFU   SYCE1   TACC2   TAF5   TBC1D12   TCERG1L   TCERG1L-AS1   TCF7L2   TCTN3   TDRD1   TECTB   TEX36   TIAL1   TLL2   TLX1   TLX1NB   TM9SF3   TRIM8   TRUB1   TUBGCP2   TWNK   UBTD1   UROS   UTF1   VAX1   VENTX   VTI1A   VWA2   WBP1L   WDR11   WNT8B   XPNPEP1   ZDHHC16   ZDHHC6   ZFYVE27   ZNF511   ZNF518A   ZRANB1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371094,346,520 - 135,427,143CLINVAR
Cytogenetic Map1010q23.33-26.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13796378
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.