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Items: 1 to 20 of 942

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124444copy number variation1nstd186human GRCh37 chr21: 47,778,821-47,779,638 , GRCh38.p12 chr21: 46,358,906-46,359,723 PCNT
    nsv5974020insertion1nstd209human GRCh38 chr21: 46,359,490-46,359,490 , GRCh37.p13 chr21: 47,779,405-47,779,405 PCNT
    nsv5966515copy number variation1nstd209human GRCh38 chr21: 46,384,712-46,384,782 , GRCh37.p13 chr21: 47,804,627-47,804,697 PCNT
    nsv5963502copy number variation1nstd209human GRCh38 chr21: 46,429,275-46,429,355 , GRCh37.p13 chr21: 47,849,189-47,849,269 PCNT
    nsv5963432copy number variation1nstd209human GRCh38 chr21: 46,371,782-46,371,868 , GRCh37.p13 chr21: 47,791,697-47,791,783 PCNT
    nsv5961841copy number variation1nstd209human GRCh38 chr21: 46,404,431-46,404,514 , GRCh37.p13 chr21: 47,824,345-47,824,428 PCNT
    nsv5961781copy number variation1nstd209human GRCh38 chr21: 46,333,398-46,334,113 , GRCh37.p13 chr21: 47,753,312-47,754,027 PCNT
    nsv5961578copy number variation1nstd209human GRCh38 chr21: 46,359,203-46,359,736 , GRCh37.p13 chr21: 47,779,118-47,779,651 PCNT
    nsv5961176copy number variation1nstd209human GRCh38 chr21: 46,381,963-46,384,685 , GRCh37.p13 chr21: 47,801,878-47,804,600 PCNT
    nsv5961122copy number variation1nstd209human GRCh38 chr21: 46,382,824-46,383,027 , GRCh37.p13 chr21: 47,802,739-47,802,942 PCNT
    nsv5959555copy number variation1nstd209human GRCh38 chr21: 46,381,998-46,384,671 , GRCh37.p13 chr21: 47,801,913-47,804,586 PCNT
    nsv5955089copy number variation1nstd209human GRCh38 chr21: 46,403,893-46,404,122 , GRCh37.p13 chr21: 47,823,807-47,824,036 PCNT
    nsv5953971copy number variation1nstd209human GRCh38 chr21: 46,365,835-46,365,898 , GRCh37.p13 chr21: 47,785,750-47,785,813 PCNT
    nsv5951545copy number variation1nstd209human GRCh38 chr21: 46,382,952-46,383,999 , GRCh37.p13 chr21: 47,802,867-47,803,914 PCNT
    nsv5951409copy number variation1nstd209human GRCh38 chr21: 46,378,287-46,378,348 , GRCh37.p13 chr21: 47,798,202-47,798,263 PCNT
    nsv5950772copy number variation1nstd209human GRCh38 chr21: 46,434,832-46,564,680 , GRCh37.p13 chr21: 47,854,745-47,984,593 DIP2A, RNU6-396P, 2 more genes
    nsv5886275copy number variation1nstd209human GRCh38 chr21: 46,436,389-46,443,494 , GRCh37.p13 chr21: 47,856,302-47,863,407 PCNT
    nsv5880963copy number variation1nstd209human GRCh38 chr21: 46,437,707-46,439,706 , GRCh37.p13 chr21: 47,857,620-47,859,619 PCNT
    nsv5697019mobile element insertion1nstd211human GRCh38 chr21: 46,343,672-46,343,672 , GRCh37.p13 chr21: 47,763,586-47,763,586 PCNT
    nsv5672515insertion2nstd207human GRCh38 chr21: 46,423,741-46,423,741 , GRCh37.p13 chr21: 47,843,655-47,843,655 PCNT
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