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Items: 1 to 20 of 379

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968000inversion1nstd209human GRCh38 chr22: 23,676,272-24,601,321 , GRCh37.p13 chr22: 24,018,459-24,997,288 , ADORA2A, 38 more genes
    nsv5958899copy number variation1nstd209human GRCh38 chr22: 22,653,852-24,634,860 , GRCh37.p13 chr22: 22,996,322-25,030,827 , LOC105372957, 122 more genes
    nsv5956621copy number variation1nstd209human GRCh38 chr22: 22,621,614-24,637,144 , GRCh37.p13 chr22: 22,964,084-25,033,111 , IGLV2-5, 125 more genes
    nsv5952967copy number variation1nstd209human GRCh38 chr22: 24,605,091-24,605,197 , GRCh37.p13 chr22: 25,001,058-25,001,164 GGT1
    nsv5671737insertion1nstd207human GRCh38 chr22: 24,605,822-24,605,822 , GRCh37.p13 chr22: 25,001,789-25,001,789 GGT1
    nsv5671715insertion1nstd207human GRCh38 chr22: 24,605,592-24,605,592 , GRCh37.p13 chr22: 25,001,559-25,001,559 GGT1
    nsv5604289copy number variation1nstd207human GRCh38 chr22: 24,605,182-24,605,317 , GRCh37.p13 chr22: 25,001,149-25,001,284 GGT1
    nsv5594036copy number variation1nstd207human GRCh38 chr22: 24,605,966-24,606,033 , GRCh37.p13 chr22: 25,001,933-25,002,000 GGT1
    nsv5589645copy number variation1nstd207human GRCh38 chr22: 24,620,040-24,620,105 , GRCh37.p13 chr22: 25,016,007-25,016,072 GGT1
    nsv5588872copy number variation1nstd207human GRCh38 chr22: 24,605,036-24,605,087 , GRCh37.p13 chr22: 25,001,003-25,001,054 GGT1
    nsv5588695copy number variation1nstd207human GRCh38 chr22: 24,608,125-24,608,675 , GRCh37.p13 chr22: 25,004,092-25,004,642 GGT1
    nsv5588547copy number variation1nstd207human GRCh38 chr22: 24,611,566-24,611,616 , GRCh37.p13 chr22: 25,007,533-25,007,583 GGT1
    nsv5587464copy number variation1nstd207human GRCh38 chr22: 24,605,614-24,605,669 , GRCh37.p13 chr22: 25,001,581-25,001,636 GGT1
    nsv5586350copy number variation1nstd207human GRCh38 chr22: 24,612,500-24,612,825 , GRCh37.p13 chr22: 25,008,467-25,008,792 GGT1
    nsv5585789copy number variation1nstd207human GRCh38 chr22: 24,605,406-24,605,522 , GRCh37.p13 chr22: 25,001,373-25,001,489 GGT1
    nsv5549806insertion1nstd206human GRCh38 chr22: 24,610,291-24,610,341 , GRCh37.p13 chr22: 25,006,258-25,006,308 GGT1
    nsv5535298copy number variation1nstd206human GRCh38 chr22: 24,611,564-24,660,000 , GRCh37.p13 chr22: 25,007,531-25,055,967 BCRP3, POM121L10P, 1 more genes
    nsv5381087copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,699,269-24,992,266 , GRCh38.p12 chr22: 23,357,082-24,596,299 LOC100129358, VPREB3, 49 more genes
    nsv5298733copy number variation1nstd204human GRCh38.p13 chr22: 24,605,301-24,605,700 , GRCh37.p13 chr22: 25,001,268-25,001,667 GGT1
    nsv5296609copy number variation1nstd204human GRCh38.p13 chr22: 24,602,601-24,606,200 , GRCh37.p13 chr22: 24,998,568-25,002,167 GGT1
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