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Variant : CV606261 (GRCh37/hg19 16p13.2(chr16:8013796-8913804)x3) Homo sapiens

Symbol: CV606261
Name: GRCh37/hg19 16p13.2(chr16:8013796-8913804)x3
Condition: not provided [RCV000751561]
Clinical Significance: benign
Last Evaluated: 11/27/2015
Review Status: no assertion criteria provided
Related Genes: ABAT   METTL22   PMM2   TMEM114   TMEM186  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37168,013,796 - 8,913,804CLINVAR
Cytogenetic Map1616p13.2CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14366887
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-05
Status: ACTIVE


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