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Variant : CV436342 (GRCh37/hg19 11q22.1-22.3(chr11:98515900-104970876)x1) Homo sapiens

Symbol: CV436342
Name: GRCh37/hg19 11q22.1-22.3(chr11:98515900-104970876)x1
Condition: See cases [RCV000511844]
Clinical Significance: likely pathogenic
Last Evaluated: 04/22/2014
Review Status: no assertion criteria provided
Related Genes: ANGPTL5   ARHGAP42   BIRC2   BIRC3   CARD16   CARD17   CASP1   CASP12   CASP4   CASP5   CEP126   CFAP300   CNTN5   DCUN1D5   DDI1   DYNC2H1   MMP1   MMP10   MMP12   MMP13   MMP20   MMP27   MMP3   MMP7   MMP8   PDGFD   PGR   TMEM123   TRPC6   YAP1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371198,515,900 - 104,970,876CLINVAR
Cytogenetic Map1111q22.1-22.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444813
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-10-08
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.