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Variant : CV380931 (GRCh37/hg19 16p13.2(chr16:8861856-8891690)x3) Homo sapiens

Symbol: CV380931
Name: GRCh37/hg19 16p13.2(chr16:8861856-8891690)x3
Condition: See cases [RCV000448659]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABAT   PMM2   TMEM186  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37168,861,856 - 8,891,690CLINVAR
Cytogenetic Map1616p13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853364
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-11-05
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.