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Variant : CV803646 (GRCh37/hg19 11q13.2(chr11:66820585-67979510)x3) Homo sapiens

Symbol: CV803646
Name: GRCh37/hg19 11q13.2(chr11:66820585-67979510)x3
Condition: not provided [RCV001006414]
Clinical Significance: uncertain significance
Last Evaluated: 12/14/2018
Review Status: no assertion criteria provided
Related Genes: ACY3   AIP   ALDH3B1   ALDH3B2   ANKRD13D   C11orf72   CABP2   CABP4   CARNS1   CDK2AP2   CHKA   CLCF1   CORO1B   GPR152   GRK2   GSTP1   KDM2A   KMT5B   NDUFS8   NDUFV1   NUDT8   PITPNM1   POLD4   PPP1CA   PTPRCAP   RAD9A   RHOD   RPS6KB2   SSH3   TBC1D10C   TBX10   TCIRG1   TMEM134   UNC93B1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371166,820,585 - 67,979,510CLINVAR
Cytogenetic Map1111q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25321870
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-10-20
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.