U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 125

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870661copy number variation1nstd102humanBenign GRCh37 chr1: 3,406,791-3,440,753 , GRCh38.p12 chr1: 3,490,227-3,524,189 MEGF6
    nsv3876250copy number variation1nstd102humanBenign GRCh37 chr1: 3,410,942-3,440,753 , GRCh38.p12 chr1: 3,494,378-3,524,189 MEGF6
    nsv3880403copy number variation1nstd102humannot provided GRCh38 chr1: 3,494,849-3,514,671 , GRCh37 chr1: 3,411,413-3,431,235 MEGF6
    esv3648623copy number variation1estd216humannot provided GRCh38.p12 chr1: 3,494,849-3,514,671 , GRCh37 chr1: 3,411,413-3,431,235 MEGF6
    nsv3881060copy number variation1nstd102humanBenign GRCh37 chr1: 3,362,256-3,417,211 , GRCh38.p12 chr1: 3,445,692-3,500,647 MEGF6, ARHGEF16
    nsv3883141copy number variation1nstd102humanBenign GRCh37 chr1: 3,362,256-3,416,173 , GRCh38.p12 chr1: 3,445,692-3,499,609 MEGF6, ARHGEF16
    nsv3885908copy number variation1nstd102humanBenign GRCh37 chr1: 3,389,727-3,423,467 , GRCh38.p12 chr1: 3,473,163-3,506,903 MEGF6, ARHGEF16
    nsv3881167copy number variation1nstd102humanBenign GRCh37 chr1: 3,393,037-3,423,467 , GRCh38.p12 chr1: 3,476,473-3,506,903 MEGF6, ARHGEF16
    nsv3875036copy number variation1nstd102humanBenign GRCh37 chr1: 3,393,037-3,418,462 , GRCh38.p12 chr1: 3,476,473-3,501,898 MEGF6, ARHGEF16
    nsv3888942copy number variation1nstd102humanBenign GRCh37 chr1: 3,393,037-3,417,211 , GRCh38.p12 chr1: 3,476,473-3,500,647 MEGF6, ARHGEF16
    nsv3918422copy number variation1nstd102humanUncertain significance NCBI36 chr1: 3,520,900-3,618,624 , GRCh37.p13 chr1: 3,531,040-3,628,764 , GRCh38.p12 chr1: 3,614,476-3,712,200 MEGF6, WRAP73, 3 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 MEGF6, RPL9P11, 466 more genes
    nsv3900501copy number variation1nstd102humanPathogenic GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016 MEGF6, MFFP1, 364 more genes
    nsv3873030copy number variation1nstd102humanPathogenic GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663 MEGF6, RN7SL451P, 376 more genes
    nsv3888433copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316 MEGF6, AURKAIP1, 356 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 MEGF6, PARK7, 325 more genes
    nsv3899046copy number variation1nstd102humanPathogenic GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775 MEGF6, PRKCZ-DT, 315 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 MEGF6, VWA1, 311 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 MEGF6, VAMP3, 245 more genes
    nsv4436631copy number variation1nstd102humanPathogenic GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784 MEGF6, LINC02606, 253 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center