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Variant : CV158765 (GRCh38/hg38 11q24.2(chr11:124565941-125095785)x1) Homo sapiens

Symbol: CV158765
Name: GRCh38/hg38 11q24.2(chr11:124565941-125095785)x1
Condition: See cases [RCV000138074]
Clinical Significance: uncertain significance
Last Evaluated: 01/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AP000866.1   AP000866.2   CCDC15   ESAM   HEPACAM   HEPN1   MSANTD2   NRGN   OR8A1   PANX3   ROBO3   ROBO4   SIAE   SLC37A2   SPA17   TBRG1   TMEM218   VSIG2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_124565941)_(125095785_?)del
NC_000011.9:g.(?_124435837)_(124965681_?)del
NC_000011.8:g.(?_123941047)_(124470891_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3811124,565,941 - 125,095,785CLINVAR
GRCh3711124,435,837 - 124,965,681CLINVAR
Build 3611123,941,047 - 124,470,891CLINVAR
Cytogenetic Map1111q24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485623
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.