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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969578insertion1nstd209human GRCh38 chr15: 83,051,867-83,051,867 , GRCh37.p13 chr15: 83,720,619-83,720,619 BTBD1
    nsv5942431copy number variation1nstd209human GRCh38 chr15: 82,965,866-83,024,030 , GRCh37.p13 chr15: 83,634,618-83,692,782 HOMER2, BTBD1, 2 more genes
    nsv5939093copy number variation1nstd209human GRCh38 chr15: 83,056,655-83,056,706 , GRCh37.p13 chr15: 83,725,407-83,725,458 BTBD1
    nsv5862194copy number variation1nstd209human GRCh38 chr15: 83,013,657-83,016,156 , GRCh37.p13 chr15: 83,682,409-83,684,908 BTBD1
    nsv5707441mobile element insertion2nstd211human GRCh38 chr15: 83,018,645-83,018,645 , GRCh37.p13 chr15: 83,687,397-83,687,397 BTBD1
    nsv5526355copy number variation1nstd206human GRCh38 chr15: 83,051,449-83,052,950 , GRCh37.p13 chr15: 83,720,201-83,721,702 BTBD1
    nsv5516159copy number variation1nstd206human GRCh38 chr15: 82,880,664-83,048,892 , GRCh37.p13 chr15: 83,549,416-83,717,644 HOMER2, BTBD1, 4 more genes
    nsv5514686copy number variation1nstd206human GRCh38 chr15: 83,038,288-83,039,109 , GRCh37.p13 chr15: 83,707,040-83,707,861 BTBD1
    nsv5428552mobile element insertion1nstd206human GRCh38 chr15: 83,018,645-83,018,696 , GRCh37.p13 chr15: 83,687,397-83,687,448 BTBD1
    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
    nsv5349231translocation1nstd200human GRCh38 chr15: 83,029,432-83,029,432 , GRCh38 chr15: 83,029,743-83,029,743 , GRCh37.p13 chr15: 83,698,495-83,698,495 , GRCh37.p13 chr15: 83,698,184-83,698,184 BTBD1
    nsv5310563copy number variation1nstd204human GRCh38.p13 chr15: 83,041,979-83,042,245 , GRCh37.p13 chr15: 83,710,731-83,710,997 BTBD1
    nsv5309581copy number variation1nstd204human GRCh38.p13 chr15: 83,022,626-83,030,290 , GRCh37.p13 chr15: 83,691,378-83,699,042 BTBD1
    nsv5274796copy number variation1nstd204human GRCh38.p13 chr15: 83,023,490-83,030,275 , GRCh37.p13 chr15: 83,692,242-83,699,027 BTBD1
    nsv5158398mobile element insertion1nstd203human GRCh38 chr15: 83,052,797-83,052,821 , GRCh37.p13 chr15: 83,721,549-83,721,573 BTBD1
    nsv5155210mobile element insertion1nstd203human GRCh38 chr15: 83,052,513-83,052,524 , GRCh37.p13 chr15: 83,721,265-83,721,276 BTBD1
    nsv5152689mobile element insertion1nstd203human GRCh38 chr15: 83,025,199-83,025,241 , GRCh37.p13 chr15: 83,693,951-83,693,993 BTBD1
    nsv5149700mobile element insertion1nstd203human GRCh38 chr15: 83,018,631-83,018,640 , GRCh37.p13 chr15: 83,687,383-83,687,392 BTBD1
    nsv5002054copy number variation1nstd200human GRCh38 chr15: 83,067,019-83,068,202 , GRCh37.p13 chr15: 83,735,771-83,736,954 BTBD1, MIR4515
    nsv5002053copy number variation1nstd200human GRCh38 chr15: 83,051,755-83,051,915 , GRCh37.p13 chr15: 83,720,507-83,720,667 BTBD1
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