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Variant : CV160674 (GRCh38/hg38 11q24.3-25(chr11:128867946-133086998)x1) Homo sapiens

Symbol: CV160674
Name: GRCh38/hg38 11q24.3-25(chr11:128867946-133086998)x1
Condition: See cases [RCV000139715]
Clinical Significance: likely pathogenic
Last Evaluated: 06/05/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAMTS15   ADAMTS8   AP003025.1   APLP2   ARHGAP32   BARX2   C11orf45   KCNJ5   LINC00167   LINC01395   LINC02551   LINC02873   MIR8052   NFRKB   NTM   NTM-AS1   NTM-IT   OPCML   PRDM10   SNX19   ST14   TMEM45B   TP53AIP1   ZBTB44   ZBTB44-DT  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_128867946)_(133086998_?)del
NC_000011.9:g.(?_128737841)_(132956893_?)del
NC_000011.8:g.(?_128243051)_(132462103_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3811128,867,946 - 133,086,998CLINVAR
GRCh3711128,737,841 - 132,956,893CLINVAR
Build 3611128,243,051 - 132,462,103CLINVAR
Cytogenetic Map1111q24.3-25CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487245
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.