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Variant : CV675899 (GRCh37/hg19 14q32.33(chr14:105708746-106020555)x3) Homo sapiens

Symbol: CV675899
Name: GRCh37/hg19 14q32.33(chr14:105708746-106020555)x3
Condition: not provided [RCV000848998]
Clinical Significance: uncertain significance
Last Evaluated: 07/27/2018
Review Status: no assertion criteria provided
Related Genes: BRF1   BTBD6   CRIP1   CRIP2   MTA1   PACS2   TEDC1   TEX22   TMEM121  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,708,746 - 106,020,555CLINVAR
Cytogenetic Map1414q32.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980527
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
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.