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Variant : CV162346 (GRCh38/hg38 16q23.3(chr16:83529919-83921660)x3) Homo sapiens

Symbol: CV162346
Name: GRCh38/hg38 16q23.3(chr16:83529919-83921660)x3
Condition: See cases [RCV000141132]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDH13   HSBP1   MLYCD  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_83529919)_(83921660_?)dup
NC_000016.9:g.(?_83563524)_(83955265_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381683,529,919 - 83,921,660CLINVAR
GRCh371683,563,524 - 83,955,265CLINVAR
Build 361682,121,025 - 82,512,766CLINVAR
Cytogenetic Map1616q23.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488659
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.