Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV155284 (GRCh38/hg38 11q23.1(chr11:111659380-112255732)x3) Homo sapiens

Symbol: CV155284
Name: GRCh38/hg38 11q23.1(chr11:111659380-112255732)x3
Condition: See cases [RCV000134885]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ALG9   BCO2   C11orf1   C11orf52   CRYAB   DIXDC1   DLAT   FDXACB1   HSPB2   HSPB2-C11orf52   IL18   NKAPD1   PIH1D2   PLET1   PPP2R1B   PTS   SDHD   SIK2   TEX12   TIMM8B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_111659380)_(112255732_?)dup
NC_000011.9:g.(?_111530104)_(112126455_?)dup
NC_000011.8:g.(?_111035314)_(111631665_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3811111,659,380 - 112,255,732CLINVAR
GRCh3711111,530,104 - 112,126,455CLINVAR
Build 3611111,035,314 - 111,631,665CLINVAR
Cytogenetic Map1111q23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482460
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



NHLBI Logo

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