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Variant : CV154739 (GRCh38/hg38 10q26.3(chr10:133134279-133400512)x1) Homo sapiens

Symbol: CV154739
Name: GRCh38/hg38 10q26.3(chr10:133134279-133400512)x1
Condition: See cases [RCV000134391]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAM8   CALY   ECHS1   FUOM   KNDC1   MIR202   MIR202HG   MIR3944   MTG1   PAOX   PRAP1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_133134279)_(133400512_?)del
NC_000010.10:g.(?_134947783)_(135214016_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810133,134,279 - 133,400,512CLINVAR
GRCh3710134,947,783 - 135,214,016CLINVAR
Build 3610134,797,773 - 135,064,006CLINVAR
Cytogenetic Map1010q26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481971
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.