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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312813copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,460,869-141,461,502 , GRCh38.p12 chr8: 140,450,770-140,451,403 TRAPPC9
    nsv7097894copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,034,014-141,034,196 , GRCh38.p12 chr8: 140,023,917-140,024,099 TRAPPC9
    nsv6312812copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,321,327-141,321,493 , GRCh38.p12 chr8: 140,311,228-140,311,394 TRAPPC9
    nsv3874368copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 140,417,391-140,444,832 , GRCh37.p13 chr8: 141,427,490-141,454,931 TRAPPC9
    nsv3920205copy number variation1nstd102humanUncertain significance NCBI36 chr8: 141,366,732-141,472,896 , GRCh38 chr8: 140,287,451-140,393,615 , GRCh37 chr8: 141,297,550-141,403,714 TRAPPC9
    nsv6290860copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,320,475-141,375,391 , GRCh38.p12 chr8: 140,310,376-140,365,292 TRAPPC9
    nsv7097895copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,445,191-141,468,663 , GRCh38.p12 chr8: 140,435,092-140,458,564 TRAPPC9
    nsv7098164copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,468,360-141,468,663 , GRCh38.p12 chr8: 140,458,261-140,458,564 TRAPPC9
    nsv4455551copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,270,416-141,289,943 , GRCh38.p12 chr8: 140,260,317-140,279,844 TRAPPC9, LOC105375779
    nsv7097652copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,285,737-141,285,940 , GRCh38.p12 chr8: 140,275,638-140,275,841 TRAPPC9, LOC105375779
    nsv3890177copy number variation1nstd102humanLikely benign GRCh37 chr8: 141,093,504-141,180,233 , GRCh38.p12 chr8: 140,083,405-140,170,134 TRAPPC9, PEG13
    nsv4729164copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,255,310-141,355,635 , GRCh38.p12 chr8: 140,245,211-140,345,536 TRAPPC9, LOC105375779
    nsv3900983copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,016,802-141,086,121 , GRCh38.p12 chr8: 140,006,705-140,076,023 TRAPPC9, LOC100421256
    nsv7098163copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,262,856-141,321,493 , GRCh38.p12 chr8: 140,252,757-140,311,394 TRAPPC9, LOC105375779
    nsv4685710copy number variation1nstd102humanPathogenic GRCh37 chr8: 140,852,548-140,953,922 , GRCh38.p12 chr8: 139,840,305-139,941,639 TRAPPC9, LOC105375781, 1 more genes
    nsv3912857copy number variation1nstd102humanUncertain significance GRCh38 chr8: 139,969,846-140,216,465 , NCBI36 chr8: 141,049,234-141,295,746 , GRCh37 chr8: 140,980,052-141,226,564 TRAPPC9, LOC100421256, 1 more genes
    nsv3902937copy number variation1nstd102humanUncertain significance GRCh37 chr8: 140,942,613-141,160,101 , GRCh38.p12 chr8: 139,930,369-140,150,002 TRAPPC9, PEG13, 1 more genes
    nsv6313739copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,016,802-141,446,902 , GRCh38.p12 chr8: 140,006,705-140,436,803 TRAPPC9, LOC105375779, 2 more genes
    nsv4729390copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,016,802-141,446,313 , GRCh38.p12 chr8: 140,006,705-140,436,214 TRAPPC9, LOC105375779, 2 more genes
    nsv6637760copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,352,715-141,656,635 , GRCh38.p12 chr8: 140,342,616-140,646,536 TRAPPC9, LOC107986982, 3 more genes
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