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 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7095561copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,918-168,282,240 , GRCh38.p12 chr1: 167,431,681-168,313,002 GCSHP5, RNU6-1310P, 21 more genes
    nsv7043735inversion1nstd229human GRCh38 chr1: 168,215,791-168,216,468 , GRCh37.p13 chr1: 168,185,029-168,185,706 LOC107985453
    nsv6644258copy number variation1nstd229human GRCh38 chr1: 168,191,501-168,243,300 , GRCh37.p13 chr1: 168,160,739-168,212,538 RPL34P1, LOC107985453, 2 more genes
    nsv6644257copy number variation1nstd229human GRCh38 chr1: 168,176,413-168,217,111 , GRCh37.p13 chr1: 168,145,651-168,186,349 TIPRL, RPL34P1, 1 more genes
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644207copy number variation1nstd229human GRCh38 chr1: 168,180,838-168,254,478 , GRCh37.p13 chr1: 168,150,076-168,223,716 TIPRL, SFT2D2, 3 more genes
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6290598copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,741,130-168,188,082 , GRCh38.p12 chr1: 167,771,893-168,218,844 MPZL1, MIR1255B2, 8 more genes
    nsv6133937copy number variation1nstd213human GRCh37 chr1: 167,800,000-169,660,001 , GRCh38.p12 chr1: 167,830,762-169,690,860 XCL2, TBX19, 38 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133597copy number variation1nstd213human GRCh37 chr1: 167,470,000-170,370,001 , GRCh38.p12 chr1: 167,500,763-170,400,860 CD247, XCL1, 64 more genes
    nsv6133565copy number variation1nstd213human GRCh37 chr1: 164,310,000-170,640,001 , GRCh38.p12 chr1: 164,340,763-170,670,860 ATP1B1, DPT, 126 more genes
    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
    nsv5079883mobile element insertion1nstd203human GRCh38 chr1: 168,216,153-168,216,155 , GRCh37.p13 chr1: 168,185,391-168,185,393 LOC107985453
    nsv5074934mobile element insertion1nstd203human GRCh38 chr1: 168,216,135-168,216,155 , GRCh37.p13 chr1: 168,185,373-168,185,393 LOC107985453
    nsv5066716mobile element insertion1nstd203human GRCh38 chr1: 168,216,155-168,216,155 , GRCh37.p13 chr1: 168,185,393-168,185,393 LOC107985453
    nsv5066335mobile element insertion1nstd203human GRCh38 chr1: 168,216,146-168,216,155 , GRCh37.p13 chr1: 168,185,384-168,185,393 LOC107985453
    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