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Variant : CV436483 (GRCh37/hg19 Xq21.33-28(chrX:96499476-151870013)x3) Homo sapiens

Symbol: CV436483
Name: GRCh37/hg19 Xq21.33-28(chrX:96499476-151870013)x3
Condition: See cases [RCV000512365]
Clinical Significance: uncertain significance
Last Evaluated: 06/23/2014
Review Status: no assertion criteria provided
Related Genes: ACSL4   ACTRT1   ADGRG4   AFF2   AGTR2   AIFM1   AKAP14   ALG13   AMMECR1   AMOT   APLN   ARHGAP36   ARHGEF6   ARL13A   ARMCX1   ARMCX2   ARMCX3   ARMCX3-AS1   ARMCX4   ARMCX5   ARMCX5-GPRASP2   ARMCX6   ATG4A   ATP11C   ATP1B4   BCORL1   BEX1   BEX2   BEX3   BEX4   BEX5   BHLHB9   BRS3   BTK   C1GALT1C1   CAPN6   CCDC160   CD40LG   CD99L2   CDR1   CENPI   CHRDL1   CLDN2   CNGA2   COL4A5   COL4A6   CSTF2   CT45A1   CT45A2   CT45A3   CT45A5   CT45A6   CT47A1   CT47A10   CT47A11   CT47A12   CT47A2   CT47A3   CT47A4   CT47A5   CT47A6   CT47A7   CT47A8   CT47A9   CT47B1   CT55   CT83   CUL4B   CXorf51A   CXorf51B   CXorf56   CXorf66   DANT2   DCAF12L1   DCAF12L2   DCX   DIAPH2   DNAAF6   DOCK11   DRP2   ELF4   ENOX2   EOLA1   EOLA2   ESX1   F9   FAM122B   FAM122C   FAM199X   FATE1   FGF13   FHL1   FMR1   FMR1-AS1   FMR1NB   FRMD7   FRMPD3   GABRA3   GABRE   GABRQ   GLA   GLUD2   GPC3   GPC4   GPR101   GPR119   GPR50   GPR50-AS1   GPRASP1   GPRASP2   GRIA3   GUCY2F   H2BW1   H2BW2   HMGB3   HNRNPH2   HPRT1   HS6ST2   HSFX1   HSFX2   HTATSF1   HTR2C   IDS   IGSF1   IL13RA1   IL13RA2   IL1RAPL2   INTS6L   IRS4   KCNE5   KIAA1210   KLHL13   LAMP2   LDOC1   LHFPL1   LONRF3   LRCH2   LUZP4   MAGEA10   MAGEA11   MAGEA4   MAGEA5   MAGEA6   MAGEA8   MAGEA9   MAGEA9B   MAGEC1   MAGEC2   MAGEC3   MAMLD1   MAP7D3   MBNL3   MCF2   MCTS1   MID2   MIR105-1   MIR105-2   MIR106A   MIR19B2   MIR224   MIR424   MIR448   MIR503   MIR506   MIR508   MIR509-1   MIR509-3   MIR510   MMGT1   MORC4   MORF4L2   MOSPD1   MTM1   MTMR1   NDUFA1   NKAP   NKRF   NOX1   NRK   NUP62CL   NXF2   NXF2B   NXF3   NXF5   NXT2   OCRL   OR13H1   PAK3   PASD1   PCDH19   PGRMC1   PHF6   PLAC1   PLP1   PLS3   PRPS1   PRR32   PRRG3   PSMD10   PWWP3B   RAB33A   RAB40A   RAB40AL   RAB9B   RADX   RAP2C   RBM41   RBMX   RBMX2   RBMXL3   RHOXF1   RHOXF2   RHOXF2B   RIPPLY1   RNF113A   RNF128   RPL36A   RPL36A-HNRNPH2   RPL39   RTL4   RTL8A   RTL8B   RTL8C   RTL9   SAGE1   SASH3   SEPTIN6   SERPINA7   SH2D1A   SLC25A14   SLC25A43   SLC25A5   SLC25A53   SLC6A14   SLC9A6   SLITRK2   SLITRK4   SMARCA1   SMIM10   SOWAHD   SOX3   SPANXA1   SPANXA2   SPANXB1   SPANXC   SPANXD   SPANXN1   SPANXN2   SPANXN3   SPANXN4   SRPX2   STAG2   STK26   SYTL4   TAF7L   TBC1D8B   TCEAL1   TCEAL2   TCEAL3   TCEAL4   TCEAL5   TCEAL6   TCEAL7   TCEAL8   TCEAL9   TCP11X2   TENM1   TEX13A   TEX13B   TFDP3   THOC2   TIMM8A   TMEM164   TMEM185A   TMEM255A   TMEM31   TMEM35A   TMSB15A   TMSB15B   TNMD   TRMT2B   TRPC5   TRPC5OS   TSC22D3   TSPAN6   UBE2A   UBE2NL   UPF3B   USP26   UTP14A   VGLL1   VMA21   VSIG1   WDR44   XIAP   XKRX   XPNPEP2   ZBTB33   ZCCHC12   ZCCHC18   ZDHHC9   ZIC3   ZMAT1   ZNF280C   ZNF449   ZNF75D  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X96,499,476 - 151,870,013CLINVAR
Cytogenetic MapXXq21.33-28CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13445328
Created: 2017-11-07
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.