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Variant : CV674677 (GRCh37/hg19 16q23.3(chr16:83553442-83973918)x3) Homo sapiens

Symbol: CV674677
Name: GRCh37/hg19 16q23.3(chr16:83553442-83973918)x3
Condition: not provided [RCV000847793]
Clinical Significance: uncertain significance
Last Evaluated: 01/22/2018
Review Status: no assertion criteria provided
Related Genes: CDH13   HSBP1   MLYCD  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371683,553,442 - 83,973,918CLINVAR
Cytogenetic Map1616q23.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979323
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-21
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.