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 116

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911540copy number variation1nstd209human GRCh38 chr11: 63,479,655-63,485,493 , GRCh37.p13 chr11: 63,247,127-63,252,965 PLAAT5
    nsv5865922copy number variation1nstd209human GRCh38 chr11: 63,484,376-63,485,575 , GRCh37.p13 chr11: 63,251,848-63,253,047 PLAAT5
    nsv5856192copy number variation1nstd209human GRCh38 chr11: 63,479,864-63,482,751 , GRCh37.p13 chr11: 63,247,336-63,250,223 PLAAT5
    nsv5728359mobile element insertion2nstd211human GRCh38 chr11: 63,461,534-63,461,534 , GRCh37.p13 chr11: 63,229,006-63,229,006 PLAAT5
    nsv5555148mobile element insertion1nstd206human GRCh38 chr11: 63,461,534-63,461,585 , GRCh37.p13 chr11: 63,229,006-63,229,057 PLAAT5
    nsv5511663copy number variation1nstd206human GRCh38 chr11: 63,460,657-63,460,768 , GRCh37.p13 chr11: 63,228,129-63,228,240 PLAAT5
    nsv5498566copy number variation1nstd206human GRCh38 chr11: 63,483,798-63,483,868 , GRCh37.p13 chr11: 63,251,270-63,251,340 PLAAT5
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5138580mobile element insertion1nstd203human GRCh38 chr11: 63,476,096-63,476,114 , GRCh37.p13 chr11: 63,243,568-63,243,586 PLAAT5
    nsv4979751copy number variation1nstd200human GRCh38 chr11: 63,472,025-63,476,235 , GRCh37.p13 chr11: 63,239,497-63,243,707 PLAAT5
    nsv4979750copy number variation1nstd200human GRCh38 chr11: 63,461,670-63,466,740 , GRCh37.p13 chr11: 63,229,142-63,234,212 PLAAT5
    nsv4838675copy number variation1nstd200human GRCh37 chr11: 63,249,190-63,250,325 , GRCh38.p12 chr11: 63,481,718-63,482,853 PLAAT5
    nsv4830154copy number variation1nstd200human GRCh37 chr11: 63,229,142-63,234,212 , GRCh38.p12 chr11: 63,461,670-63,466,740 PLAAT5
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729316copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,714,816-63,383,226 , GRCh38.p12 chr11: 62,947,344-63,615,754 LOC105369334, PLAAT3, 18 more genes
    nsv4570044mobile element insertion1nstd166human GRCh37.p13 chr11: 63,228,991-63,228,991 , GRCh38.p12 chr11: 63,461,519-63,461,519 PLAAT5
    nsv4325349mobile element insertion1nstd166human GRCh37.p13 chr11: 63,243,883-63,243,883 , GRCh38.p12 chr11: 63,476,411-63,476,411 PLAAT5
    nsv3969050insertion1nstd168human GRCh38 chr11: 63,393,307-63,506,568 , GRCh37.p13 chr11: 63,160,779-63,274,040 LGALS12, SLC22A9, 2 more genes
    nsv3959811copy number variation1nstd168human GRCh38 chr11: 63,401,070-63,536,204 , GRCh37.p13 chr11: 63,168,542-63,303,676 PLAAT4, TMSB4XP5, 4 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