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Variant : CV165466 (GRCh38/hg38 21q21.3(chr21:26773248-29573178)x1) Homo sapiens

Symbol: CV165466
Name: GRCh38/hg38 21q21.3(chr21:26773248-29573178)x1
Condition: See cases [RCV000143779]
Clinical Significance: uncertain significance
Last Evaluated: 03/18/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAMTS1   ADAMTS5   BACH1   BACH1-IT2   BACH1-IT3   CCT8   GRIK1   LINC00113   LINC00161   LINC00189   LINC00314   LINC01673   LINC01695   LINC01697   LOC110121429   LOC112694735   LTN1   MAP3K7CL   MIR4759   N6AMT1   RWDD2B   USP16  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_26773248)_(29573178_?)del
NC_000021.8:g.(?_28145567)_(30945498_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382126,773,248 - 29,573,178CLINVAR
GRCh372128,145,567 - 30,945,498CLINVAR
Build 362127,067,438 - 29,867,369CLINVAR
Cytogenetic Map2121q21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9491377
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.