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Variant : CV435577 (GRCh37/hg19 16p12.1(chr16:25900524-27489837)x3) Homo sapiens

Symbol: CV435577
Name: GRCh37/hg19 16p12.1(chr16:25900524-27489837)x3
Condition: See cases [RCV000511134]
Clinical Significance: uncertain significance
Last Evaluated: 06/03/2014
Review Status: no assertion criteria provided
Related Genes: C16orf82   GTF3C1   HS3ST4   IL21R   IL4R   KDM8   NSMCE1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371625,900,524 - 27,489,837CLINVAR
Cytogenetic Map1616p12.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444109
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-12-03
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.