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Variant : CV162874 (GRCh38/hg38 13q34(chr13:114147230-114277653)x3) Homo sapiens

Symbol: CV162874
Name: GRCh38/hg38 13q34(chr13:114147230-114277653)x3
Condition: See cases [RCV000141622]
Clinical Significance: uncertain significance
Last Evaluated: 09/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDC16   CFAP97D2   MIR4502   MIR548AR  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_114147230)_(114277653_?)dup
NC_000013.10:g.(?_114893774)_(115043128_?)dup
NC_000013.9:g.(?_113911876)_(114061230_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3813114,147,230 - 114,277,653 (+)CLINVAR
GRCh3713114,893,774 - 115,043,128CLINVAR
Build 3613113,911,876 - 114,061,230CLINVAR
Cytogenetic Map1313q34CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489147
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.