Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV162353 (GRCh38/hg38 16p13.3(chr16:492760-565476)x3) Homo sapiens

Symbol: CV162353
Name: GRCh38/hg38 16p13.3(chr16:492760-565476)x3
Condition: See cases [RCV000141138]
Clinical Significance: benign|likely benign|conflicting data from submitters
Last Evaluated: 04/30/2011
Review Status: classified by multiple submitters|classified by single submitter|no assertion criteria provided
Related Genes: CAPN15   LINC00235   MIR3176   MIR5587   PRR35   RAB11FIP3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_492760)_(565476_?)dup
NC_000016.9:g.(?_542760)_(615476_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3816492,760 - 565,476CLINVAR
GRCh3716542,760 - 615,476CLINVAR
Build 3616482,761 - 555,477CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488665
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.