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 131

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7051881inversion1nstd229human GRCh38 chr3: 119,069,449-119,472,399 , GRCh37.p13 chr3: 118,788,296-119,191,246 B4GALT4, RNU6-1127P, 9 more genes
    nsv7049104inversion1nstd229human GRCh38 chr3: 114,751,914-119,661,867 , GRCh37.p13 chr3: 114,470,761-119,380,714 LINC00901, EIF4E2P2, 50 more genes
    nsv6714040copy number variation1nstd229human GRCh38 chr3: 119,135,323-119,250,941 , GRCh37.p13 chr3: 118,854,170-118,969,788 TEX55, B4GALT4-AS1, 3 more genes
    nsv6713840copy number variation1nstd229human GRCh38 chr3: 119,121,101-119,191,700 , GRCh37.p13 chr3: 118,839,948-118,910,547 IGSF11, TEX55, 1 more genes
    nsv6712976copy number variation1nstd229human GRCh38 chr3: 119,083,999-119,153,674 , GRCh37.p13 chr3: 118,802,846-118,872,521 IGSF11, TEX55
    nsv6712000copy number variation1nstd229human GRCh38 chr3: 119,145,555-119,149,898 , GRCh37.p13 chr3: 118,864,402-118,868,745 IGSF11, TEX55
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6701887copy number variation1nstd229human GRCh38 chr3: 119,136,526-119,283,876 , GRCh37.p13 chr3: 118,855,373-119,002,723 B4GALT4-AS1, B4GALT4, 3 more genes
    nsv6698786copy number variation1nstd229human GRCh38 chr3: 119,145,601-119,149,900 , GRCh37.p13 chr3: 118,864,448-118,868,747 TEX55, IGSF11
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6637150copy number variation1nstd102humanUncertain significance GRCh37 chr3: 116,109,191-120,328,013 , GRCh38.p12 chr3: 116,390,344-120,609,166 LOC101926953, LOC105374058, 60 more genes
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv5447678copy number variation1nstd206human GRCh38 chr3: 119,136,526-119,283,873 , GRCh37.p13 chr3: 118,855,373-119,002,720 IGSF11, UPK1B, 3 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919755copy number variation1nstd200human GRCh38 chr3: 118,773,498-119,384,319 , GRCh37.p13 chr3: 118,492,345-119,103,166 TEX55, LOC105374060, 10 more genes
    nsv4806918copy number variation1nstd200human GRCh37 chr3: 118,855,373-119,002,720 , GRCh38.p12 chr3: 119,136,526-119,283,873 TEX55, B4GALT4, 3 more genes
    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