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 246

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059858inversion1nstd229human GRCh38 chr10: 6,597,285-7,714,805 , GRCh37.p13 chr10: 6,639,247-7,756,768 LINC00707, ITIH5, 14 more genes
    nsv6897040copy number variation1nstd229human GRCh38 chr10: 7,718,990-7,721,234 , GRCh37.p13 chr10: 7,760,953-7,763,197 ITIH2
    nsv6894527copy number variation1nstd229human GRCh38 chr10: 7,708,122-7,708,200 , GRCh37.p13 chr10: 7,750,085-7,750,163 ITIH2
    nsv6893830copy number variation1nstd229human GRCh38 chr10: 7,704,020-7,714,743 , GRCh37.p13 chr10: 7,745,983-7,756,706 ITIH2
    nsv6892836copy number variation1nstd229human GRCh38 chr10: 7,707,697-7,714,098 , GRCh37.p13 chr10: 7,749,660-7,756,061 ITIH2
    nsv6890154copy number variation1nstd229human GRCh38 chr10: 7,731,510-7,743,157 , GRCh37.p13 chr10: 7,773,473-7,785,120 ITIH2
    nsv6887212copy number variation1nstd229human GRCh38 chr10: 7,710,996-7,711,023 , GRCh37.p13 chr10: 7,752,959-7,752,986 ITIH2
    nsv6883369copy number variation1nstd229human GRCh38 chr10: 7,727,517-7,727,823 , GRCh37.p13 chr10: 7,769,480-7,769,786 ITIH2
    nsv6637939copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,027-12,648,149 , GRCh38.p12 chr10: 54,087-12,606,150 LARP4B-DT, CALML5, 206 more genes
    nsv6637674copy number variation1nstd102humanUncertain significance GRCh37 chr10: 7,636,590-11,590,970 , GRCh38.p12 chr10: 7,594,627-11,548,971 HSP90AB7P, LOC105376394, 41 more genes
    nsv6620426copy number variation1nstd224human GRCh37 chr10: 7,716,641-7,766,958 , GRCh38.p12 chr10: 7,674,678-7,724,995 ITIH2
    nsv6581361inversion1nstd223human GRCh38 chr10: 7,730,967-7,731,451 , GRCh37.p13 chr10: 7,772,930-7,773,414 ITIH2
    nsv6445606copy number variation1nstd223human GRCh38 chr10: 7,718,490-7,719,779 , GRCh37.p13 chr10: 7,760,453-7,761,742 ITIH2
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6184855copy number variation1nstd214human GRCh38 chr10: 7,737,687-7,737,746 , GRCh37.p13 chr10: 7,779,650-7,779,709 ITIH2
    nsv6168280copy number variation1nstd214human GRCh38 chr10: 7,737,674-7,737,781 , GRCh37.p13 chr10: 7,779,637-7,779,744 ITIH2
    nsv6131971copy number variation1nstd213human GRCh37 chr10: 7,450,000-17,830,001 , GRCh38.p12 chr10: 7,408,038-17,788,002 ATP5F1C, TRDMT1, 150 more genes
    nsv6100251insertion1nstd212human GRCh38 chr10: 7,737,662-7,737,662 , GRCh37.p13 chr10: 7,779,625-7,779,625 ITIH2
    nsv6091717insertion1nstd212human GRCh38 chr10: 7,738,165-7,738,165 , GRCh37.p13 chr10: 7,780,128-7,780,128 ITIH2
    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