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Variant : CV605849 (GRCh37/hg19 14q32.33(chr14:105932544-106072470)x3) Homo sapiens

Symbol: CV605849
Name: GRCh37/hg19 14q32.33(chr14:105932544-106072470)x3
Condition: not provided [RCV000751149]
Clinical Significance: benign
Last Evaluated: 03/15/2013
Review Status: no assertion criteria provided
Related Genes: CRIP1   CRIP2   IGH   IGHA2   IGHE   MTA1   TEDC1   TMEM121  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3714105,932,544 - 106,072,470CLINVAR
Cytogenetic Map1414q32.33CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14366475
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE


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