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Variant : CV163478 (GRCh38/hg38 8p21.2(chr8:24017764-24642890)x3) Homo sapiens

Symbol: CV163478
Name: GRCh38/hg38 8p21.2(chr8:24017764-24642890)x3
Condition: See cases [RCV000142014]
Clinical Significance: uncertain significance
Last Evaluated: 08/26/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC024958.1   ADAM28   ADAM7   ADAMDEC1   LOC101929294   LOC113788272  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_24017764)_(24642890_?)dup
NC_000008.10:g.(?_23875277)_(24500403_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38824,017,764 - 24,642,890CLINVAR
GRCh37823,875,277 - 24,500,403CLINVAR
Build 36823,931,222 - 24,556,293CLINVAR
Cytogenetic Map88p21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489534
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-10-20
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.