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Variant : CV603965 (GRCh37/hg19 1q25.3-41(chr1:185644663-221698833)x3) Homo sapiens

Symbol: CV603965
Name: GRCh37/hg19 1q25.3-41(chr1:185644663-221698833)x3
Condition: not provided [RCV000749265]
Clinical Significance: pathogenic
Last Evaluated: 05/29/2012
Review Status: no assertion criteria provided
Related Genes: ADIPOR1   ADORA1   ANGEL2   ARL8A   ASCL5   ASPM   ATF3   ATP2B4   ATP6V1G3   AVPR1B   B3GALT2   BATF3   BPNT1   BRINP3   BTG2   C1orf115   C1orf116   C1orf147   C1orf53   C1orf74   C4BPA   C4BPB   CACNA1S   CAMK1G   CAMSAP2   CD34   CD46   CD55   CDC73   CDK18   CENPF   CFH   CFHR1   CFHR2   CFHR3   CFHR4   CFHR5   CHI3L1   CHIT1   CNTN2   CR1   CR1L   CR2   CRB1   CSRP1   CTSE   CYB5R1   DDX59   DENND1B   DSTYK   DTL   DYRK3   EIF2D   ELF3   ELK4   EPRS1   ESRRG   ETNK2   F13B   FAM71A   FAM72A   FCAMR   FCMR   FLVCR1   FLVCR1-DT   FMOD   G0S2   GLRX2   GOLT1A   GPATCH2   GPR25   GPR37L1   HHAT   HLX   HMCN1   HSD11B1   IARS2   IGFN1   IKBKE   IL10   IL19   IL20   IL24   INAVA   INTS7   IPO9   IRF6   KCNH1   KCNK2   KCNT2   KCTD3   KDM5B   KIF14   KIF21B   KISS1   KLHDC8A   KLHL12   LAD1   LAMB3   LAX1   LEMD1   LGR6   LHX9   LINC00538   LMOD1   LPGAT1   LRRN2   LYPLAL1   MAPKAPK2   MARK1   MDM4   MFSD4A   MIR181A1   MIR181B1   MIR194-1   MIR205   MIR205HG   MIR215   MIR29B2CHG   MIR29C   MTARC1   MTARC2   MYBPH   MYOG   NAV1   NEK2   NEK7   NENF   NFASC   NR5A2   NSL1   NUAK2   NUCKS1   OCLM   ODR4   OPTC   PACC1   PCAT6   PDC   PFKFB2   PHLDA3   PIGR   PIK3C2B   PKP1   PLA2G4A   PLEKHA6   PLXNA2   PM20D1   PPFIA4   PPP1R12B   PPP1R15B   PPP2R5A   PRELP   PRG4   PROX1   PTGS2   PTPN14   PTPN7   PTPRC   RAB29   RAB3GAP2   RABIF   RASSF5   RBBP5   RCOR3   RD3   REN   RGS1   RGS13   RGS18   RGS2   RGS21   RHEX   RNPEP   RO60   RPS6KC1   RRP15   SERTAD4   SHISA4   SLC26A9   SLC30A1   SLC30A10   SLC41A1   SLC45A3   SMYD2   SNRPE   SOX13   SPATA17   SPATA45   SRGAP2   SYT14   SYT2   TATDN3   TGFB2   TIMM17A   TMCC2   TMEM183A   TMEM81   TMEM9   TNNI1   TNNT2   TPR   TRAF3IP3   TRAF5   UBE2T   UCHL5   USH2A   UTP25   VASH2   YOD1   ZBED6   ZBTB41   ZC3H11A   ZNF281  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371185,644,663 - 221,698,833CLINVAR
Cytogenetic Map11q25.3-41CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14364596
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-08
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.