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Items: 1 to 20 of 477

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5962284insertion1nstd209human GRCh38 chr2: 85,308,376-85,308,376 , GRCh37.p13 chr2: 85,535,499-85,535,499 TCF7L1
    nsv5881431copy number variation1nstd209human GRCh38 chr2: 85,240,849-85,240,949 , GRCh37.p13 chr2: 85,467,972-85,468,072 , TCF7L1
    nsv5880993copy number variation1nstd209human GRCh38 chr2: 85,152,649-85,152,735 , GRCh37.p13 chr2: 85,379,772-85,379,858 TCF7L1
    nsv5880571copy number variation1nstd209human GRCh38 chr2: 85,291,705-85,292,301 , GRCh37.p13 chr2: 85,518,828-85,519,424 TCF7L1
    nsv5879238copy number variation1nstd209human GRCh38 chr2: 85,291,982-85,292,318 , GRCh37.p13 chr2: 85,519,105-85,519,441 TCF7L1
    nsv5870421copy number variation1nstd209human GRCh38 chr2: 85,299,361-85,301,924 , GRCh37.p13 chr2: 85,526,484-85,529,047 TCF7L1
    nsv5868452copy number variation1nstd209human GRCh38 chr2: 85,299,489-85,299,795 , GRCh37.p13 chr2: 85,526,612-85,526,918 TCF7L1
    nsv5833826copy number variation1nstd209human GRCh38 chr2: 85,298,944-85,301,786 , GRCh37.p13 chr2: 85,526,067-85,528,909 TCF7L1
    nsv5833757copy number variation2nstd209human GRCh38 chr2: 85,298,943-85,300,086 , GRCh37.p13 chr2: 85,526,066-85,527,209 TCF7L1
    nsv5719487mobile element insertion1nstd211human GRCh38 chr2: 85,191,055-85,191,055 , GRCh37.p13 chr2: 85,418,178-85,418,178 TCF7L1
    nsv5681754mobile element insertion1nstd211human GRCh38 chr2: 85,167,096-85,167,096 , GRCh37.p13 chr2: 85,394,219-85,394,219 TCF7L1
    nsv5609688insertion2nstd207human GRCh38 chr2: 85,308,385-85,308,385 , GRCh37.p13 chr2: 85,535,508-85,535,508 TCF7L1
    nsv5609146insertion1nstd207human GRCh38 chr2: 85,294,331-85,294,331 , GRCh37.p13 chr2: 85,521,454-85,521,454 TCF7L1
    nsv5604975insertion1nstd207human GRCh38 chr2: 85,191,043-85,191,043 , GRCh37.p13 chr2: 85,418,166-85,418,166 TCF7L1
    nsv5578610copy number variation1nstd207human GRCh38 chr2: 85,152,649-85,152,735 , GRCh37.p13 chr2: 85,379,772-85,379,858 TCF7L1
    nsv5575936copy number variation1nstd207human GRCh38 chr2: 85,291,982-85,292,318 , GRCh37.p13 chr2: 85,519,105-85,519,441 TCF7L1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5447109copy number variation1nstd206human GRCh38 chr2: 85,299,349-85,301,979 , GRCh37.p13 chr2: 85,526,472-85,529,102 TCF7L1
    nsv5439528copy number variation1nstd206human GRCh38 chr2: 85,184,759-85,184,827 , GRCh37.p13 chr2: 85,411,882-85,411,950 TCF7L1, TCF7L1-IT1
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