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Variant : CV158260 (GRCh38/hg38 11q25(chr11:131212028-135075271)x1) Homo sapiens

Symbol: CV158260
Name: GRCh38/hg38 11q25(chr11:131212028-135075271)x1
Condition: See cases [RCV000137583]
Clinical Significance: pathogenic
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACAD8   AP003025.1   B3GAT1   B3GAT1-DT   GLB1L2   GLB1L3   IGSF9B   JAM3   LINC02684   LINC02697   LINC02706   LINC02714   LINC02731   LINC02743   MIR4697   NCAPD3   NTM   NTM-AS1   NTM-IT   OPCML   SNORD153   SPATA19   THYN1   VPS26B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_131212028)_(135075271_?)del
NC_000011.9:g.(?_131081923)_(134945165_?)del
NC_000011.8:g.(?_130587133)_(134450377_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3811131,212,028 - 135,075,271CLINVAR
GRCh3711131,081,923 - 134,945,165CLINVAR
Build 3611130,587,133 - 134,450,377CLINVAR
Cytogenetic Map1111q25CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485137
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.