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 666

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6113598mobile element insertion1nstd186human GRCh37 chr21: 18,992,116-18,992,167 , GRCh38.p12 chr21|NT_187627.1: 16,104-16,155 , GRCh38.p12 chr21: 17,619,798-17,619,849 CXADR
    nsv5972973insertion1nstd209human GRCh38 chr21: 17,619,780-17,619,780 , GRCh37.p13 chr21: 18,992,098-18,992,098 CXADR
    nsv5969026insertion1nstd209human GRCh38 chr21: 17,563,940-17,563,940 , GRCh37.p13 chr21: 18,936,258-18,936,258 CXADR
    nsv5965857copy number variation1nstd209human GRCh38 chr21: 14,377,888-22,678,896 , GRCh37.p13 chr21: 15,750,209-24,051,216 , LOC107985508, 80 more genes
    nsv5961610copy number variation1nstd209human GRCh38 chr21: 17,528,321-17,528,654 , GRCh37.p13 chr21: 18,900,639-18,900,972 CXADR
    nsv5952615copy number variation1nstd209human GRCh38 chr21: 17,600,231-17,600,280 , GRCh37.p13 chr21: 18,972,549-18,972,598 BTG3, CXADR
    nsv5701722mobile element insertion2nstd211human GRCh38 chr21: 17,619,798-17,619,798 , GRCh37.p13 chr21: 18,992,116-18,992,116 CXADR
    nsv5696159mobile element insertion1nstd211human GRCh38 chr21: 17,561,700-17,561,700 , GRCh37.p13 chr21: 18,934,018-18,934,018 CXADR
    nsv5667917insertion1nstd207human GRCh38 chr21: 17,619,780-17,619,780 , GRCh37.p13 chr21: 18,992,098-18,992,098 CXADR
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5532209copy number variation1nstd206human GRCh38 chr21: 17,516,262-17,516,393 , GRCh37.p13 chr21: 18,888,580-18,888,711 CXADR, BTF3L4P1
    nsv5526808copy number variation1nstd206human GRCh38 chr21: 17,532,491-17,532,565 , GRCh37.p13 chr21: 18,904,809-18,904,883 CXADR
    nsv5523478copy number variation1nstd206human GRCh38 chr21: 17,550,210-17,551,184 , GRCh37.p13 chr21: 18,922,528-18,923,502 CXADR
    nsv5516406copy number variation1nstd206human GRCh38 chr21: 17,591,243-17,592,685 , GRCh37.p13 chr21: 18,963,561-18,965,003 CXADR, BTG3
    nsv5432410mobile element insertion1nstd206human GRCh38 chr21: 17,619,798-17,619,849 , GRCh37.p13 chr21: 18,992,116-18,992,167 CXADR
    nsv5423109mobile element insertion1nstd206human GRCh38 chr21: 17,561,700-17,561,751 , GRCh37.p13 chr21: 18,934,018-18,934,069 CXADR
    nsv5350627translocation1nstd200human GRCh38 chr21: 17,546,243-17,546,243 , GRCh38 chr21: 17,545,718-17,545,718 , GRCh37.p13 chr21: 18,918,561-18,918,561 , GRCh37.p13 chr21: 18,918,036-18,918,036 CXADR
    nsv5347260translocation1nstd200human GRCh38 chr21: 17,567,383-17,567,383 , GRCh38 chr7: 83,231,173-83,231,173 , GRCh37.p13 chr21: 18,939,701-18,939,701 , GRCh37.p13 chr7: 82,860,489-82,860,489 CXADR
    nsv5328919copy number variation1nstd204human GRCh38.p13 chr21: 17,576,359-17,576,774 , GRCh37.p13 chr21: 18,948,677-18,949,092 CXADR
    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