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 161

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5964626insertion1nstd209human GRCh38 chr6: 132,706,868-132,706,868 , GRCh37.p13 chr6: 133,028,007-133,028,007 VNN1
    nsv5898950copy number variation1nstd209human GRCh38 chr6: 132,692,645-132,692,703 , GRCh37.p13 chr6: 133,013,784-133,013,842 VNN1
    nsv5726285mobile element insertion2nstd211human GRCh38 chr6: 132,706,883-132,706,883 , GRCh37.p13 chr6: 133,028,022-133,028,022 VNN1
    nsv5641746insertion1nstd207human GRCh38 chr6: 132,706,868-132,706,868 , GRCh37.p13 chr6: 133,028,007-133,028,007 VNN1
    nsv5461799copy number variation1nstd206human GRCh38 chr6: 132,692,645-132,692,711 , GRCh37.p13 chr6: 133,013,784-133,013,850 VNN1
    nsv5369773translocation1nstd200human GRCh38 chr6: 132,692,645-132,692,645 , GRCh38 chr6: 132,692,711-132,692,711 , GRCh37.p13 chr6: 133,013,784-133,013,784 , GRCh37.p13 chr6: 133,013,850-133,013,850 VNN1
    nsv5336841translocation1nstd200human GRCh37 chr6: 133,013,784-133,013,784 , GRCh37 chr6: 133,013,850-133,013,850 , GRCh38.p12 chr6: 132,692,711-132,692,711 , GRCh38.p12 chr6: 132,692,645-132,692,645 VNN1
    nsv5199333mobile element insertion1nstd203human GRCh38 chr6: 132,706,875-132,706,883 , GRCh37.p13 chr6: 133,028,014-133,028,022 VNN1
    nsv5192462mobile element insertion1nstd203human GRCh38 chr6: 132,706,868-132,706,883 , GRCh37.p13 chr6: 133,028,007-133,028,022 VNN1
    nsv5189338mobile element insertion1nstd203human GRCh38 chr6: 132,706,873-132,706,883 , GRCh37.p13 chr6: 133,028,012-133,028,022 VNN1
    nsv5188227mobile element insertion1nstd203human GRCh38 chr6: 132,706,867-132,706,883 , GRCh37.p13 chr6: 133,028,006-133,028,022 VNN1
    nsv5180273mobile element insertion1nstd203human GRCh38 chr6: 132,706,872-132,706,883 , GRCh37.p13 chr6: 133,028,011-133,028,022 VNN1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945689copy number variation1nstd200human GRCh38 chr6: 132,661,447-132,706,146 , GRCh37.p13 chr6: 132,982,586-133,027,285 HLFP1, CCNG1P1, 1 more genes
    nsv4934170copy number variation1nstd200human GRCh38 chr6: 132,697,066-132,697,884 , GRCh37.p13 chr6: 133,018,205-133,019,023 VNN1, CCNG1P1
    nsv4767747insertion1nstd199human GRCh37 chr6: 133,028,016-133,028,016 , GRCh38.p12 chr6: 132,706,877-132,706,877 VNN1
    nsv4743548copy number variation1nstd199human GRCh37 chr6: 133,013,780-133,013,844 , GRCh38.p12 chr6: 132,692,641-132,692,705 VNN1
    nsv4725217insertion1nstd186human GRCh37 chr6: 133,028,007-133,028,007 , GRCh38.p12 chr6: 132,706,868-132,706,868 VNN1
    nsv4698144mobile element insertion1nstd186human GRCh37 chr6: 133,028,022-133,028,022 , GRCh38.p12 chr6: 132,706,883-132,706,883 VNN1
    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