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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114033mobile element insertion1nstd186human GRCh37 chr12: 52,685,503-52,685,554 , GRCh38.p12 chr12: 52,291,719-52,291,770 KRT81, KRT86
    nsv5977932insertion1nstd209human GRCh38 chr12: 52,291,701-52,291,701 , GRCh37.p13 chr12: 52,685,485-52,685,485 KRT86, KRT81
    nsv5701449mobile element insertion2nstd211human GRCh38 chr12: 52,291,719-52,291,719 , GRCh37.p13 chr12: 52,685,503-52,685,503 KRT81, KRT86
    nsv5660726insertion1nstd207human GRCh38 chr12: 52,291,701-52,291,701 , GRCh37.p13 chr12: 52,685,485-52,685,485 KRT81, KRT86
    nsv5510341copy number variation1nstd206human GRCh38 chr12: 52,289,022-52,289,097 , GRCh37.p13 chr12: 52,682,806-52,682,881 KRT86, KRT81
    nsv5432866mobile element insertion1nstd206human GRCh38 chr12: 52,291,719-52,291,770 , GRCh37.p13 chr12: 52,685,503-52,685,554 KRT86, KRT81
    nsv5136333mobile element insertion1nstd203human GRCh38 chr12: 52,291,705-52,291,719 , GRCh37.p13 chr12: 52,685,489-52,685,503 KRT86, KRT81
    nsv5133891mobile element insertion1nstd203human GRCh38 chr12: 52,291,704-52,291,715 , GRCh37.p13 chr12: 52,685,488-52,685,499 KRT86, KRT81
    nsv5129913mobile element insertion1nstd203human GRCh38 chr12: 52,291,700-52,291,715 , GRCh37.p13 chr12: 52,685,484-52,685,499 KRT86, KRT81
    nsv5127620mobile element insertion1nstd203human GRCh38 chr12: 52,291,706-52,291,719 , GRCh37.p13 chr12: 52,685,490-52,685,503 KRT86, KRT81
    nsv5125943mobile element insertion1nstd203human GRCh38 chr12: 52,291,701-52,291,719 , GRCh37.p13 chr12: 52,685,485-52,685,503 KRT86, KRT81
    nsv5122150mobile element insertion1nstd203human GRCh38 chr12: 52,291,708-52,291,719 , GRCh37.p13 chr12: 52,685,492-52,685,503 KRT81, KRT86
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4972708copy number variation1nstd200human GRCh38 chr12: 52,284,230-52,286,309 , GRCh37.p13 chr12: 52,678,014-52,680,093 KRT81, KRT86
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4753524insertion1nstd199human GRCh37 chr12: 52,685,491-52,685,491 , GRCh38.p12 chr12: 52,291,707-52,291,707 KRT81, KRT86
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4718857insertion1nstd186human GRCh37 chr12: 52,685,485-52,685,485 , GRCh38.p12 chr12: 52,291,701-52,291,701 KRT86, KRT81
    nsv4688026mobile element insertion1nstd186human GRCh37 chr12: 52,685,503-52,685,503 , GRCh38.p12 chr12: 52,291,719-52,291,719 KRT81, KRT86
    nsv4614464copy number variation1nstd183human GRCh37 chr12: 52,682,239-52,779,578 , GRCh38.p12 chr12: 52,288,455-52,385,794 KRT81, KRT83, 4 more genes
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