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Variant : CV158704 (GRCh38/hg38 16q23.1(chr16:76680652-77199749)x4) Homo sapiens

Symbol: CV158704
Name: GRCh38/hg38 16q23.1(chr16:76680652-77199749)x4
Condition: See cases [RCV000138015]
Clinical Significance: uncertain significance
Last Evaluated: 12/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR4719   MON1B   SYCE1L  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_76680652)_(77199749_?)dup
NC_000016.9:g.(?_76714549)_(77233646_?)dup
NC_000016.8:g.(?_75272050)_(75791147_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381676,680,652 - 77,199,749CLINVAR
GRCh371676,714,549 - 77,233,646CLINVAR
Build 361675,272,050 - 75,791,147CLINVAR
Cytogenetic Map1616q23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485564
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.