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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309731copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,782,167-48,927,084 , GRCh38.p12 chr15: 48,489,970-48,634,887 FBN1
    nsv3878384copy number variation1nstd102humanPathogenic GRCh38 chr15: 48,410,970-48,537,828 , GRCh37 chr15: 48,703,167-48,830,025 FBN1
    nsv6309793copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,177-48,830,015 , GRCh38.p12 chr15: 48,410,980-48,537,818 FBN1
    nsv4682035copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,795,974-48,905,299 , GRCh38.p12 chr15: 48,503,777-48,613,102 FBN1
    nsv3881185copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,167-48,789,608 , GRCh38 chr15: 48,410,970-48,497,411 FBN1
    nsv1398079copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,523-48,760,718 , GRCh38 chr15: 48,411,326-48,468,521 FBN1
    nsv4682742copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,177-48,758,065 , GRCh38.p12 chr15: 48,410,980-48,465,868 FBN1
    nsv3889016copy number variation1nstd102humanPathogenic GRCh38 chr15: 48,415,161-48,468,554 , GRCh37 chr15: 48,707,358-48,760,751 FBN1
    nsv6314946copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,707,733-48,758,055 , GRCh38.p12 chr15: 48,415,536-48,465,858 FBN1
    nsv4681089copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,720,533-48,766,857 , GRCh38.p12 chr15: 48,428,336-48,474,660 FBN1
    nsv3876236copy number variation1nstd102humanPathogenic GRCh38 chr15: 48,410,990-48,456,762 , GRCh37 chr15: 48,703,187-48,748,959 FBN1
    nsv5672742copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,181-48,744,887 , GRCh38.p12 chr15: 48,410,984-48,452,690 FBN1
    nsv6309732copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,791,162-48,830,025 , GRCh38.p12 chr15: 48,498,965-48,537,828 FBN1
    nsv4452048copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,752,423-48,791,255 , GRCh38 chr15: 48,460,226-48,499,058 FBN1
    nsv7094379copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,187-48,741,110 , GRCh38.p12 chr15: 48,410,990-48,448,913 FBN1
    nsv5672667copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,795,974-48,830,015 , GRCh38.p12 chr15: 48,503,777-48,537,818 FBN1
    nsv3881192copy number variation1nstd102humanPathogenic GRCh38 chr15: 48,470,614-48,499,058 , GRCh37 chr15: 48,762,811-48,791,255 FBN1
    nsv7094714copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,729,138-48,748,979 , GRCh38.p12 chr15: 48,436,941-48,456,782 FBN1
    nsv7094382copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,888,460-48,905,309 , GRCh38.p12 chr15: 48,596,263-48,613,112 FBN1
    nsv4453921copy number variation1nstd102humanPathogenic GRCh38 chr15: 48,596,273-48,613,102 , GRCh37 chr15: 48,888,470-48,905,299 FBN1
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