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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936446copy number variation1nstd209human GRCh38 chr15: 69,286,019-69,286,089 , GRCh37.p13 chr15: 69,578,358-69,578,428 PAQR5, PAQR5-DT
    nsv5694937mobile element insertion1nstd211human GRCh38 chr15: 69,290,335-69,290,335 , GRCh37.p13 chr15: 69,582,674-69,582,674 PAQR5-DT, PAQR5
    nsv5655581insertion1nstd207human GRCh38 chr15: 69,286,019-69,286,019 , GRCh37.p13 chr15: 69,578,358-69,578,358 PAQR5-DT, PAQR5
    nsv5416804mobile element insertion1nstd206human GRCh38 chr15: 69,290,335-69,290,386 , GRCh37.p13 chr15: 69,582,674-69,582,725 PAQR5-DT, PAQR5
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5153247mobile element insertion1nstd203human GRCh38 chr15: 69,285,461-69,285,479 , GRCh37.p13 chr15: 69,577,800-69,577,818 PAQR5, PAQR5-DT
    nsv5140741mobile element insertion1nstd203human GRCh38 chr15: 69,285,471-69,285,479 , GRCh37.p13 chr15: 69,577,810-69,577,818 PAQR5-DT, PAQR5
    nsv4992187copy number variation1nstd200human GRCh38 chr15: 69,281,733-69,320,527 , GRCh37.p13 chr15: 69,574,072-69,612,866 PAQR5, PAQR5-DT
    nsv4992186copy number variation1nstd200human GRCh38 chr15: 69,281,734-69,308,818 , GRCh37.p13 chr15: 69,574,073-69,601,157 PAQR5-DT, PAQR5
    nsv4755044insertion1nstd199human GRCh37 chr15: 69,578,374-69,578,374 , GRCh38.p12 chr15: 69,286,035-69,286,035 PAQR5, PAQR5-DT
    nsv4456268copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,369,118-70,481,307 , GRCh38.p12 chr15: 67,076,780-70,188,968 ANP32A-IT1, CARS1P1, 48 more genes
    nsv4446924insertion1nstd175human GRCh37 chr15: 69,578,336-69,578,336 , GRCh38.p12 chr15: 69,285,997-69,285,997 PAQR5, PAQR5-DT
    nsv4338323sequence alteration1nstd166human GRCh37.p13 chr15: 69,446,476-72,211,091 , GRCh38.p12 chr15: 69,154,137-71,918,750 , MYO9A, 45 more genes
    nsv3925443insertion1nstd167human GRCh37 chr15: 69,578,358-69,578,358 , GRCh38.p12 chr15: 69,286,019-69,286,019 PAQR5, PAQR5-DT
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920633copy number variation1nstd102humanPathogenic GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678 NEO1, LOC390600, 95 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
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