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Variant : CV248259 (GRCh37/hg19 11q13.2(chr11:66024774-67430781)x3) Homo sapiens

Symbol: CV248259
Name: GRCh37/hg19 11q13.2(chr11:66024774-67430781)x3
Condition: See cases [RCV000240374]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ACTN3   ACY3   AIP   ALDH3B2   ANKRD13D   B4GAT1   BBS1   BRMS1   C11orf72   C11orf80   C11orf86   CABP2   CABP4   CARNS1   CCDC87   CCS   CD248   CDK2AP2   CLCF1   CNIH2   CORO1B   CTSF   DPP3   GPR152   GRK2   GSTP1   KDM2A   KLC2   LRFN4   MRPL11   NDUFV1   NPAS4   NUDT8   PC   PELI3   PITPNM1   POLD4   PPP1CA   PTPRCAP   RAB1B   RAD9A   RBM14   RBM14-RBM4   RBM4   RBM4B   RCE1   RHOD   RIN1   RPS6KB2   SLC29A2   SPTBN2   SSH3   SYT12   TBC1D10C   TBX10   TMEM134   TMEM151A   YIF1A   ZDHHC24  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371166,024,774 - 67,430,781CLINVAR
Cytogenetic Map1111q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11541781
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-10-15
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.