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Variant : CV160878 (GRCh38/hg38 8q24.12(chr8:118626991-119703035)x3) Homo sapiens

Symbol: CV160878
Name: GRCh38/hg38 8q24.12(chr8:118626991-119703035)x3
Condition: See cases [RCV000139886]
Clinical Significance: uncertain significance
Last Evaluated: 02/20/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CCN3   COLEC10   ENPP2   MAL2   MAL2-AS1   MIR548AZ   SAMD12-AS1   TNFRSF11B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_118626991)_(119703035_?)dup
NC_000008.10:g.(?_119639230)_(120715275_?)dup
NC_000008.9:g.(?_119708411)_(120784456_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388118,626,991 - 119,703,035CLINVAR
GRCh378119,639,230 - 120,715,275CLINVAR
Build 368119,708,411 - 120,784,456CLINVAR
Cytogenetic Map88q24.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487416
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-31
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.