U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 227

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076748inversion1nstd229human GRCh38 chr19: 45,264,764-45,374,993 , GRCh37.p13 chr19: 45,768,022-45,878,251 KLC3, MARK4, 3 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7072733inversion1nstd229human GRCh38 chr19: 45,188,785-45,379,046 , GRCh37.p13 chr19: 45,692,043-45,882,304 PPP1R13L, RPS16P9, 7 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7015772copy number variation1nstd229human GRCh38 chr19: 45,241,201-45,249,500 , GRCh37.p13 chr19: 45,744,459-45,752,758 MARK4
    nsv7010070copy number variation1nstd229human GRCh38 chr19: 45,282,456-45,286,475 , GRCh37.p13 chr19: 45,785,714-45,789,733 MARK4
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7000766copy number variation1nstd229human GRCh38 chr19: 45,287,512-45,288,633 , GRCh37.p13 chr19: 45,790,770-45,791,891 MARK4
    nsv6598902inversion1nstd223human GRCh38 chr19: 45,275,140-45,276,188 , GRCh37.p13 chr19: 45,778,398-45,779,446 MARK4
    nsv6523815copy number variation1nstd223human GRCh38 chr19: 44,276,620-45,370,613 , GRCh37.p13 chr19: 44,780,773-45,873,871 APOE, CEACAM16, 48 more genes
    nsv6517058copy number variation1nstd223human GRCh38 chr19: 45,287,512-45,288,633 , GRCh37.p13 chr19: 45,790,770-45,791,891 MARK4
    nsv6314081copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,074,342-46,133,841 , GRCh38.p12 chr19: 44,571,096-45,630,583 EXOC3L2, APOE, 50 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv6103268inversion1nstd212human GRCh38 chr19: 45,080,087-46,509,008 , GRCh37.p13 chr19: 45,583,345-47,012,265 , CKM, 72 more genes
    nsv5942239copy number variation1nstd209human GRCh38 chr19: 45,222,223-45,249,559 , GRCh37.p13 chr19: 45,725,481-45,752,817 MARK4, EXOC3L2, 1 more genes
    nsv5933264copy number variation1nstd209human GRCh38 chr19: 45,279,816-45,280,165 , GRCh37.p13 chr19: 45,783,074-45,783,423 MARK4
    nsv5523920copy number variation1nstd206human GRCh38 chr19: 45,291,496-45,291,564 , GRCh37.p13 chr19: 45,794,754-45,794,822 MARK4
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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