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Variant : CV605848 (GRCh37/hg19 14q32.33(chr14:105871769-106327640)x3) Homo sapiens

Symbol: CV605848
Name: GRCh37/hg19 14q32.33(chr14:105871769-106327640)x3
Condition: not provided [RCV000751148]
Clinical Significance: benign
Last Evaluated: 07/02/2014
Review Status: no assertion criteria provided
Related Genes: CRIP1   CRIP2   IGH   IGHA1   IGHA2   IGHD   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   MTA1   TEDC1   TEX22   TMEM121  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3714105,871,769 - 106,327,640CLINVAR
Cytogenetic Map1414q32.33CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14366474
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


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