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Variant : CV381930 (GRCh37/hg19 11q24.2(chr11:124254553-125315622)x1) Homo sapiens

Symbol: CV381930
Name: GRCh37/hg19 11q24.2(chr11:124254553-125315622)x1
Condition: See cases [RCV000448684]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CCDC15   ESAM   HEPACAM   HEPN1   MSANTD2   NRGN   OR8A1   OR8B12   OR8B3   OR8B4   OR8B8   PANX3   PKNOX2   ROBO3   ROBO4   SIAE   SLC37A2   SPA17   TBRG1   TMEM218   VSIG2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711124,254,553 - 125,315,622CLINVAR
Cytogenetic Map1111q24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853388
Created: 2017-04-11
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.