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Variant : CV157177 (GRCh38/hg38 8p21.2(chr8:23757449-24517207)x3) Homo sapiens

Symbol: CV157177
Name: GRCh38/hg38 8p21.2(chr8:23757449-24517207)x3
Condition: See cases [RCV000136617]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC024958.1   ADAM28   ADAM7   ADAMDEC1   LOC101929294   LOC113788271   LOC113788272   STC1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_23757449)_(24517207_?)dup
NC_000008.10:g.(?_23614962)_(24374720_?)dup
NC_000008.9:g.(?_23670907)_(24430610_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38823,757,449 - 24,517,207CLINVAR
GRCh37823,614,962 - 24,374,720CLINVAR
Build 36823,670,907 - 24,430,610CLINVAR
Cytogenetic Map88p21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484178
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-10-15
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.