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Variant : CV435306 (GRCh37/hg19 14q32.33(chr14:105587643-106560949)x3) Homo sapiens

Symbol: CV435306
Name: GRCh37/hg19 14q32.33(chr14:105587643-106560949)x3
Condition: See cases [RCV000512193]
Clinical Significance: likely benign
Last Evaluated: 02/29/2016
Review Status: no assertion criteria provided
Related Genes: BRF1   BTBD6   CRIP1   CRIP2   IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   JAG2   MTA1   NUDT14   PACS2   TEDC1   TEX22   TMEM121  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,587,643 - 106,560,949CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445160
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-11-12
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.