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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146984insertion1nstd232human GRCh37.p13 chr1: 168,088,496-168,088,496 , GRCh38.p12 chr1: 168,119,258-168,119,258 GPR161
    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
    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
    nsv6644204copy number variation1nstd229human GRCh38 chr1: 168,115,853-168,123,598 , GRCh37.p13 chr1: 168,085,091-168,092,836 GPR161
    nsv6644138copy number variation1nstd229human GRCh38 chr1: 168,092,847-168,096,674 , GRCh37.p13 chr1: 168,062,085-168,065,912 GPR161
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6334256copy number variation1nstd223human GRCh38 chr1: 168,108,450-168,109,827 , GRCh37.p13 chr1: 168,077,688-168,079,065 GPR161
    nsv6332338copy number variation1nstd223human GRCh38 chr1: 168,092,847-168,096,670 , GRCh37.p13 chr1: 168,062,085-168,065,908 GPR161
    nsv6332141copy number variation1nstd223human GRCh38 chr1: 168,105,474-168,107,829 , GRCh37.p13 chr1: 168,074,712-168,077,067 GPR161
    nsv6329476copy number variation1nstd223human GRCh38 chr1: 168,119,802-168,122,236 , GRCh37.p13 chr1: 168,089,040-168,091,474 GPR161
    nsv6326754copy number variation1nstd223human GRCh38 chr1: 168,106,386-168,119,506 , GRCh37.p13 chr1: 168,075,624-168,088,744 GPR161
    nsv6316251copy number variation1nstd223human GRCh38 chr1: 168,109,268-168,110,762 , GRCh37.p13 chr1: 168,078,506-168,080,000 GPR161
    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
    nsv6149524copy number variation1nstd214human GRCh38 chr1: 168,119,215-168,119,276 , GRCh37.p13 chr1: 168,088,453-168,088,514 GPR161
    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
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