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Variant : CV155183 (GRCh38/hg38 11q12.3(chr11:62562836-62840570)x3) Homo sapiens

Symbol: CV155183
Name: GRCh38/hg38 11q12.3(chr11:62562836-62840570)x3
Condition: See cases [RCV000134807]
Clinical Significance: uncertain significance
Last Evaluated: 09/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: B3GAT3   BSCL2   C11orf98   CSKMT   EEF1G   EML3   GANAB   GNG3   HNRNPUL2   HNRNPUL2-BSCL2   INTS5   LBHD1   LRRN4CL   MIR6514   MIR6747   MIR6748   MTA2   NXF1   POLR2G   ROM1   SNORA57   STX5   TAF6L   TMEM179B   TMEM223   TTC9C   TUT1   UBXN1   UQCC3   WDR74   ZBTB3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_62562836)_(62840570_?)dup
NC_000011.9:g.(?_62330308)_(62608042_?)dup
NC_000011.8:g.(?_62086884)_(62364618_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381162,562,836 - 62,840,570CLINVAR
GRCh371162,330,308 - 62,608,042CLINVAR
Build 361162,086,884 - 62,364,618CLINVAR
Cytogenetic Map1111q12.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482384
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.