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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711071mobile element insertion1nstd211human GRCh38 chr8: 38,114,772-38,114,772 , GRCh37.p13 chr8: 37,972,290-37,972,290 ASH2L
    nsv5490999copy number variation1nstd206human GRCh38 chr8: 38,138,320-38,138,385 , GRCh37.p13 chr8: 37,995,838-37,995,903 ASH2L
    nsv5482706copy number variation1nstd206human GRCh38 chr8: 38,078,585-38,160,675 , GRCh37.p13 chr8: 37,936,103-38,018,193 LOC105379382, STAR, 2 more genes
    nsv5411043mobile element insertion1nstd206human GRCh38 chr8: 38,114,772-38,114,823 , GRCh37.p13 chr8: 37,972,290-37,972,341 ASH2L
    nsv5364081translocation1nstd200human GRCh38 chr8: 38,109,063-38,109,063 , GRCh38 chr8: 38,109,124-38,109,124 , GRCh37.p13 chr8: 37,966,642-37,966,642 , GRCh37.p13 chr8: 37,966,581-37,966,581 ASH2L
    nsv5345801translocation1nstd200human GRCh37 chr8: 37,966,642-37,966,642 , GRCh37 chr8: 37,966,581-37,966,581 , GRCh38.p12 chr8: 38,109,124-38,109,124 , GRCh38.p12 chr8: 38,109,063-38,109,063 ASH2L
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5119411mobile element insertion1nstd203human GRCh38 chr8: 38,126,853-38,126,853 , GRCh37.p13 chr8: 37,984,371-37,984,371 ASH2L
    nsv5110854mobile element insertion1nstd203human GRCh38 chr8: 38,126,858-38,126,858 , GRCh37.p13 chr8: 37,984,376-37,984,376 ASH2L
    nsv4960237copy number variation1nstd200human GRCh38 chr8: 38,112,614-38,112,868 , GRCh37.p13 chr8: 37,970,132-37,970,386 ASH2L
    nsv4954356copy number variation1nstd200human GRCh38 chr8: 38,056,730-38,123,350 , GRCh37.p13 chr8: 37,914,248-37,980,868 ASH2L, EIF4EBP1, 1 more genes
    nsv4825731copy number variation1nstd200human GRCh37 chr8: 37,914,248-37,980,868 , GRCh38.p12 chr8: 38,056,730-38,123,350 ASH2L, EIF4EBP1, 1 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4713131copy number variation1nstd195human GRCh37 chr8: 37,984,377-37,984,378 , GRCh38.p12 chr8: 38,126,859-38,126,860 ASH2L
    nsv4546164insertion1nstd166human GRCh37.p13 chr8: 37,987,140-37,987,140 , GRCh38.p12 chr8: 38,129,622-38,129,622 ASH2L
    nsv4489524mobile element insertion1nstd166human GRCh37.p13 chr8: 37,982,789-37,982,789 , GRCh38.p12 chr8: 38,125,271-38,125,271 ASH2L
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4436744copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,486,830-37,992,515 , GRCh38.p12 chr8: 36,629,312-38,134,997 LOC105379380, LOC728024, 29 more genes
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