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Variant : CV605845 (GRCh37/hg19 14q32.33(chr14:105436222-107287663)x3) Homo sapiens

Symbol: CV605845
Name: GRCh37/hg19 14q32.33(chr14:105436222-107287663)x3
Condition: not provided [RCV000751145]
Clinical Significance: benign
Last Evaluated: 03/06/2013
Review Status: no assertion criteria provided
Related Genes: AHNAK2   BRF1   BTBD6   CDCA4   CLBA1   CRIP1   CRIP2   GPR132   IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   IGHV3-23   JAG2   MTA1   NUDT14   PACS2   TEDC1   TEX22   TMEM121  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,436,222 - 107,287,663CLINVAR
Cytogenetic Map1414q32.33CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366471
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-08-04
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.