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Items: 1 to 20 of 254

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094050copy number variation1nstd102humanUncertain significance GRCh37 chr12: 52,862,846-52,865,100 , GRCh38.p12 chr12: 52,469,062-52,471,316 KRT6C
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7061604inversion1nstd229human GRCh38 chr12: 52,288,016-52,732,145 , GRCh37.p13 chr12: 52,681,800-53,125,929 KRT81, LOC400036, 22 more genes
    nsv6929037copy number variation1nstd229human GRCh38 chr12: 52,469,917-52,488,556 , GRCh37.p13 chr12: 52,863,701-52,882,340 KRT6A, KRT6C
    nsv6928980copy number variation1nstd229human GRCh38 chr12: 52,472,101-52,473,500 , GRCh37.p13 chr12: 52,865,885-52,867,284 KRT6C
    nsv6621821copy number variation1nstd224human GRCh37 chr12: 52,863,032-52,886,513 , GRCh38.p12 chr12: 52,469,248-52,492,729 KRT6C, KRT6A
    nsv6621709copy number variation1nstd224human GRCh37 chr12: 52,649,887-53,071,246 , GRCh38.p12 chr12: 52,256,103-52,677,462 KRT1, KRT6B, 21 more genes
    nsv6465790copy number variation1nstd223human GRCh38 chr12: 52,448,940-52,490,060 , GRCh37.p13 chr12: 52,842,724-52,883,844 KRT6A, KRT6B, 1 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132426copy number variation1nstd213human GRCh37 chr12: 52,740,000-55,260,001 , GRCh38.p12 chr12: 52,346,216-54,866,217 , HOXC4, 122 more genes
    nsv5946419copy number variation1nstd209human GRCh38 chr12: 52,452,326-52,473,893 , GRCh37.p13 chr12: 52,846,110-52,867,677 KRT6B, KRT6C
    nsv5865423copy number variation2nstd209human GRCh38 chr12: 52,467,705-52,469,054 , GRCh37.p13 chr12: 52,861,489-52,862,838 KRT6C
    nsv5864309copy number variation1nstd209human GRCh38 chr12: 52,470,565-52,471,895 , GRCh37.p13 chr12: 52,864,349-52,865,679 KRT6C
    nsv5861199copy number variation1nstd209human GRCh38 chr12: 52,459,322-52,466,554 , GRCh37.p13 chr12: 52,853,106-52,860,338 KRT6C
    nsv5860109copy number variation1nstd209human GRCh38 chr12: 52,451,511-52,471,745 , GRCh37.p13 chr12: 52,845,295-52,865,529 KRT6C, KRT6B
    nsv5859161copy number variation1nstd209human GRCh38 chr12: 52,466,405-52,467,904 , GRCh37.p13 chr12: 52,860,189-52,861,688 KRT6C
    nsv5849874copy number variation1nstd209human GRCh38 chr12: 52,473,286-52,491,754 , GRCh37.p13 chr12: 52,867,070-52,885,538 KRT6A, KRT6C
    nsv5496812copy number variation1nstd206human GRCh38 chr12: 52,448,955-52,490,050 , GRCh37.p13 chr12: 52,842,739-52,883,834 KRT6A, KRT6B, 1 more genes
    nsv5495150copy number variation1nstd206human GRCh38 chr12: 52,452,000-52,473,000 , GRCh37.p13 chr12: 52,845,784-52,866,784 KRT6B, KRT6C
    nsv5278388copy number variation1nstd204human GRCh38.p13 chr12: 52,472,101-52,472,600 , GRCh37.p13 chr12: 52,865,885-52,866,384 KRT6C
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