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Variant : CV155408 (GRCh38/hg38 13q12.11-12.12(chr13:22091310-23146964)x3) Homo sapiens

Symbol: CV155408
Name: GRCh38/hg38 13q12.11-12.12(chr13:22091310-23146964)x3
Condition: See cases [RCV000134984]
Clinical Significance: likely benign
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00540   LINC00621  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_22091310)_(23146964_?)dup
NC_000013.10:g.(?_22665449)_(23721103_?)dup
NC_000013.9:g.(?_21563449)_(22619103_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381322,091,310 - 23,146,964CLINVAR
GRCh371322,665,449 - 23,721,103CLINVAR
Build 361321,563,449 - 22,619,103CLINVAR
Cytogenetic Map1313q12.11-12.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482557
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.