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Variant : CV613897 (GRCh37/hg19 11q13.1-13.2(chr11:65138976-67574402)) Homo sapiens

Symbol: CV613897
Name: GRCh37/hg19 11q13.1-13.2(chr11:65138976-67574402)
Condition: not provided [RCV000767601]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: ACTN3   ACY3   AIP   ALDH3B2   ANKRD13D   AP5B1   B4GAT1   BANF1   BBS1   BRMS1   C11orf68   C11orf72   C11orf80   C11orf86   CABP2   CABP4   CARNS1   CATSPER1   CCDC85B   CCDC87   CCS   CD248   CDK2AP2   CFL1   CLCF1   CNIH2   CORO1B   CST6   CTSF   CTSW   DPP3   DRAP1   EFEMP2   EHBP1L1   EIF1AD   FAM89B   FIBP   FOSL1   FRMD8   GAL3ST3   GPR152   GRK2   GSTP1   KAT5   KCNK7   KDM2A   KLC2   LRFN4   LTBP3   MALAT1   MAP3K11   MRPL11   MUS81   NDUFV1   NEAT1   NPAS4   NUDT8   OVOL1   PACS1   PC   PCNX3   PELI3   PITPNM1   POLD4   PPP1CA   PTPRCAP   RAB1B   RAD9A   RBM14   RBM14-RBM4   RBM4   RBM4B   RCE1   RELA   RHOD   RIN1   RNASEH2C   RPS6KB2   SART1   SCYL1   SF3B2   SIPA1   SLC25A45   SLC29A2   SNX32   SPTBN2   SSH3   SYT12   TBC1D10C   TBX10   TMEM134   TMEM151A   TSGA10IP   YIF1A   ZDHHC24   ZNRD2  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371165,138,976 - 67,574,402CLINVAR
Cytogenetic Map1111q13.1-13.2CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 14399568
Created: 2019-05-07
Species: Homo sapiens
Last Modified: 2020-10-20
Status: ACTIVE


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