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Variant : CV159735 (GRCh38/hg38 13q34(chr13:114245917-114293574)x3) Homo sapiens

Symbol: CV159735
Name: GRCh38/hg38 13q34(chr13:114245917-114293574)x3
Condition: See cases [RCV000138912]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDC16   MIR4502   UPF3A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_114245917)_(114293574_?)dup
NC_000013.10:g.(?_115011392)_(115059049_?)dup
NC_000013.9:g.(?_114029494)_(114077151_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3813114,245,917 - 114,293,574CLINVAR
GRCh3713115,011,392 - 115,059,049CLINVAR
Build 3613114,029,494 - 114,077,151CLINVAR
Cytogenetic Map1313q34CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486444
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.