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 157

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955066insertion1nstd209human GRCh38 chr1: 155,147,380-155,147,380 , GRCh37.p13 chr1: 155,119,856-155,119,856 HMGN2P18
    nsv5690976mobile element insertion1nstd211human GRCh38 chr1: 155,146,795-155,146,795 , GRCh37.p13 chr1: 155,119,271-155,119,271 HMGN2P18
    nsv5614543insertion1nstd207human GRCh38 chr1: 155,147,390-155,147,390 , GRCh37.p13 chr1: 155,119,866-155,119,866 HMGN2P18
    nsv5612028insertion2nstd207human GRCh38 chr1: 155,147,380-155,147,380 , GRCh37.p13 chr1: 155,119,856-155,119,856 HMGN2P18
    nsv5562447inversion1nstd206human GRCh38 chr1: 155,147,381-155,147,440 , GRCh37.p13 chr1: 155,119,857-155,119,916 HMGN2P18
    nsv5433347copy number variation1nstd206human GRCh38 chr1: 155,146,790-155,154,164 , GRCh37.p13 chr1: 155,119,266-155,126,640 HMGN2P18
    nsv5431760copy number variation1nstd206human GRCh38 chr1: 155,147,352-155,147,442 , GRCh37.p13 chr1: 155,119,828-155,119,918 HMGN2P18
    nsv5430216copy number variation1nstd206human GRCh38 chr1: 155,149,863-155,149,930 , GRCh37.p13 chr1: 155,122,339-155,122,406 HMGN2P18
    nsv5423972copy number variation1nstd206human GRCh38 chr1: 155,047,651-155,175,025 , GRCh37.p13 chr1: 155,020,127-155,147,501 DCST1, EFNA4, 9 more genes
    nsv5408323mobile element insertion1nstd206human GRCh38 chr1: 155,146,795-155,146,833 , GRCh37.p13 chr1: 155,119,271-155,119,309 HMGN2P18
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5211686copy number variation1nstd204human GRCh38.p13 chr1: 153,974,901-155,189,600 , GRCh37.p13 chr1: 153,947,377-155,161,231 JTB, PYGO2-AS1, 56 more genes
    nsv5203279copy number variation1nstd204human GRCh38.p13 chr1: 154,942,701-155,189,300 , GRCh37.p13 chr1: 154,915,177-155,160,979 MUC1, MIR4258, 21 more genes
    nsv5069008mobile element insertion1nstd203human GRCh38 chr1: 155,146,784-155,146,795 , GRCh37.p13 chr1: 155,119,260-155,119,271 HMGN2P18
    nsv5062000mobile element insertion1nstd203human GRCh38 chr1: 155,146,777-155,146,795 , GRCh37.p13 chr1: 155,119,253-155,119,271 HMGN2P18
    nsv4897522copy number variation1nstd200human GRCh38 chr1: 155,147,238-155,154,166 , GRCh37.p13 chr1: 155,119,714-155,126,642 HMGN2P18
    nsv4784295copy number variation1nstd200human GRCh37 chr1: 155,119,714-155,126,642 , GRCh38.p12 chr1: 155,147,238-155,154,166 HMGN2P18
    nsv4784294copy number variation1nstd200human GRCh37 chr1: 155,119,821-155,119,898 , GRCh38.p12 chr1: 155,147,345-155,147,422 HMGN2P18
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4766617insertion1nstd199human GRCh37 chr1: 155,119,836-155,119,836 , GRCh38.p12 chr1: 155,147,360-155,147,360 HMGN2P18
    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