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Variant : CV161800 (GRCh38/hg38 10q26.3(chr10:133059029-133622588)x3) Homo sapiens

Symbol: CV161800
Name: GRCh38/hg38 10q26.3(chr10:133059029-133622588)x3
Condition: See cases [RCV000140708]
Clinical Significance: uncertain significance
Last Evaluated: 11/26/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAM8   ADGRA1   ADGRA1-AS1   CALY   CYP2E1   ECHS1   FUOM   KNDC1   MIR202   MIR202HG   MIR3944   MTG1   PAOX   PRAP1   SPRN   SYCE1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_133059029)_(133622588_?)dup
NC_000010.10:g.(?_134872533)_(135436092_?)dup
NC_000010.9:g.(?_134722523)_(135286082_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3810133,059,029 - 133,622,588CLINVAR
GRCh3710134,872,533 - 135,436,092CLINVAR
Build 3610134,722,523 - 135,286,082CLINVAR
Cytogenetic Map1010q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488237
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.