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    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
    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
    nsv6644208copy number variation1nstd229human GRCh38 chr1: 168,195,402-168,200,843 , GRCh37.p13 chr1: 168,164,640-168,170,081 TIPRL
    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
    nsv6644141copy number variation1nstd229human GRCh38 chr1: 168,180,870-168,181,417 , GRCh37.p13 chr1: 168,150,108-168,150,655 TIPRL
    nsv6643767copy number variation1nstd229human GRCh38 chr1: 168,201,801-168,205,200 , GRCh37.p13 chr1: 168,171,039-168,174,438 TIPRL
    nsv6548470inversion1nstd223human GRCh38 chr1: 168,188,866-168,188,984 , GRCh37.p13 chr1: 168,158,104-168,158,222 TIPRL
    nsv6542208inversion1nstd223human GRCh38 chr1: 168,176,622-168,177,590 , GRCh37.p13 chr1: 168,145,860-168,146,828 TIPRL
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6537019inversion1nstd223human GRCh38 chr1: 168,181,443-168,181,781 , GRCh37.p13 chr1: 168,150,681-168,151,019 TIPRL
    nsv6327840copy number variation1nstd223human GRCh38 chr1: 168,186,071-168,188,317 , GRCh37.p13 chr1: 168,155,309-168,157,555 TIPRL
    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
    nsv6245574mobile element insertion1nstd215human GRCh38 chr1: 168,182,878-168,182,878 , GRCh37.p13 chr1: 168,152,116-168,152,116 TIPRL
    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
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