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Variant : CV160322 (GRCh38/hg38 10q21.1(chr10:57200350-57512400)x1) Homo sapiens

Symbol: CV160322
Name: GRCh38/hg38 10q21.1(chr10:57200350-57512400)x1
Condition: See cases [RCV000139409]
Clinical Significance: likely benign
Last Evaluated: 04/05/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR3924  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_57200350)_(57512400_?)del
NC_000010.10:g.(?_58960110)_(59272160_?)del
NC_000010.9:g.(?_58630116)_(58942166_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381057,200,350 - 57,512,400CLINVAR
GRCh371058,960,110 - 59,272,160CLINVAR
Build 361058,630,116 - 58,942,166CLINVAR
Cytogenetic Map1010q21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486940
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-17
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.