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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713871mobile element insertion1nstd211human GRCh38 chr15: 88,835,049-88,835,049 , GRCh37.p13 chr15: 89,378,280-89,378,280 ACAN
    nsv5708644mobile element insertion2nstd211human GRCh38 chr15: 88,813,327-88,813,327 , GRCh37.p13 chr15: 89,356,558-89,356,558 ACAN
    nsv5660479insertion2nstd207human GRCh38 chr15: 88,855,709-88,855,709 , GRCh37.p13 chr15: 89,398,940-89,398,940 ACAN
    nsv5658435insertion1nstd207human GRCh38 chr15: 88,856,267-88,856,267 , GRCh37.p13 chr15: 89,399,498-89,399,498 ACAN
    nsv5648246insertion1nstd207human GRCh38 chr15: 88,855,507-88,855,507 , GRCh37.p13 chr15: 89,398,738-89,398,738 ACAN
    nsv5604195copy number variation1nstd207human GRCh38 chr15: 88,855,823-88,856,164 , GRCh37.p13 chr15: 89,399,054-89,399,395 ACAN
    nsv5597571copy number variation1nstd207human GRCh38 chr15: 88,855,507-88,855,563 , GRCh37.p13 chr15: 89,398,738-89,398,794 ACAN
    nsv5564525insertion1nstd102humanUncertain significance GRCh38 chr15: 88,856,755-88,856,755 , GRCh37 chr15: 89,399,986-89,399,986 ACAN
    nsv5529671copy number variation1nstd206human GRCh38 chr15: 88,855,496-88,855,746 , GRCh37.p13 chr15: 89,398,727-89,398,977 ACAN
    nsv5521611copy number variation1nstd206human GRCh38 chr15: 88,855,597-88,856,837 , GRCh37.p13 chr15: 89,398,828-89,400,068 ACAN
    nsv5421130mobile element insertion1nstd206human GRCh38 chr15: 88,813,327-88,813,378 , GRCh37.p13 chr15: 89,356,558-89,356,609 ACAN
    nsv5417851mobile element insertion1nstd206human GRCh38 chr15: 88,835,049-88,835,100 , GRCh37.p13 chr15: 89,378,280-89,378,331 ACAN
    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
    nsv5365414translocation1nstd200human GRCh38 chr15: 88,820,034-88,820,034 , GRCh38 chr15: 88,824,092-88,824,092 , GRCh37.p13 chr15: 89,367,323-89,367,323 , GRCh37.p13 chr15: 89,363,265-89,363,265 ACAN
    nsv5365413translocation1nstd200human GRCh38 chr15: 88,819,738-88,819,738 , GRCh38 chr15: 88,820,821-88,820,821 , GRCh37.p13 chr15: 89,364,052-89,364,052 , GRCh37.p13 chr15: 89,362,969-89,362,969 ACAN
    nsv5349270translocation1nstd200human GRCh38 chr15: 88,784,841-88,784,841 , GRCh38 chr15: 88,823,455-88,823,455 , GRCh37.p13 chr15: 89,328,072-89,328,072 , GRCh37.p13 chr15: 89,366,686-89,366,686 ACAN
    nsv5339184translocation1nstd200human GRCh37 chr15: 89,366,686-89,366,686 , GRCh37 chr15: 89,328,072-89,328,072 , GRCh38.p12 chr15: 88,823,455-88,823,455 , GRCh38.p12 chr15: 88,784,841-88,784,841 ACAN
    nsv5338654translocation1nstd200human GRCh37 chr15: 89,367,323-89,367,323 , GRCh37 chr15: 89,363,265-89,363,265 , GRCh38.p12 chr15: 88,820,034-88,820,034 , GRCh38.p12 chr15: 88,824,092-88,824,092 ACAN
    nsv5333990translocation1nstd200human GRCh37 chr15: 89,362,974-89,362,974 , GRCh37 chr15: 89,364,052-89,364,052 , GRCh38.p12 chr15: 88,819,743-88,819,743 , GRCh38.p12 chr15: 88,820,821-88,820,821 ACAN
    nsv5312159copy number variation1nstd204human GRCh38.p13 chr15: 88,804,342-88,822,070 , GRCh37.p13 chr15: 89,347,573-89,365,301 ACAN
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