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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130931insertion1nstd186human GRCh37 chr12: 121,490,574-121,490,574 , GRCh38.p12 chr12: 121,052,771-121,052,771 OASL2P
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5647565insertion1nstd207human GRCh38 chr12: 121,052,762-121,052,762 , GRCh37.p13 chr12: 121,490,565-121,490,565 OASL2P
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv5537958insertion1nstd206human GRCh38 chr12: 121,052,771-121,052,771 , GRCh37.p13 chr12: 121,490,574-121,490,574 OASL2P
    nsv5136694mobile element insertion1nstd203human GRCh38 chr12: 121,052,749-121,052,780 , GRCh37.p13 chr12: 121,490,552-121,490,583 OASL2P
    nsv5136263mobile element insertion1nstd203human GRCh38 chr12: 121,052,705-121,052,780 , GRCh37.p13 chr12: 121,490,508-121,490,583 OASL2P
    nsv5133633mobile element insertion1nstd203human GRCh38 chr12: 121,052,522-121,052,522 , GRCh37.p13 chr12: 121,490,325-121,490,325 OASL2P
    nsv5132815mobile element insertion1nstd203human GRCh38 chr12: 121,052,765-121,052,778 , GRCh37.p13 chr12: 121,490,568-121,490,581 OASL2P
    nsv5129843mobile element insertion1nstd203human GRCh38 chr12: 121,052,746-121,052,780 , GRCh37.p13 chr12: 121,490,549-121,490,583 OASL2P
    nsv5128118mobile element insertion1nstd203human GRCh38 chr12: 121,052,750-121,052,779 , GRCh37.p13 chr12: 121,490,553-121,490,582 OASL2P
    nsv5127444mobile element insertion1nstd203human GRCh38 chr12: 121,052,476-121,052,476 , GRCh37.p13 chr12: 121,490,279-121,490,279 OASL2P
    nsv5124948mobile element insertion1nstd203human GRCh38 chr12: 121,052,780-121,052,789 , GRCh37.p13 chr12: 121,490,583-121,490,592 OASL2P
    nsv5122979mobile element insertion1nstd203human GRCh38 chr12: 121,052,740-121,052,780 , GRCh37.p13 chr12: 121,490,543-121,490,583 OASL2P
    nsv5122804mobile element insertion1nstd203human GRCh38 chr12: 121,052,771-121,052,780 , GRCh37.p13 chr12: 121,490,574-121,490,583 OASL2P
    nsv4769067insertion1nstd186human GRCh37 chr12: 121,490,553-121,490,553 , GRCh38.p12 chr12: 121,052,750-121,052,750 OASL2P
    nsv4766492insertion1nstd199human GRCh37 chr12: 121,490,568-121,490,568 , GRCh38.p12 chr12: 121,052,765-121,052,765 OASL2P
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
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