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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7066259inversion1nstd229human GRCh38 chr12: 52,645,502-52,648,661 , GRCh37.p13 chr12: 53,039,286-53,042,445 KRT2
    nsv7063308inversion1nstd229human GRCh38 chr12: 52,644,858-52,644,903 , GRCh37.p13 chr12: 53,038,642-53,038,687 KRT2
    nsv7061604inversion1nstd229human GRCh38 chr12: 52,288,016-52,732,145 , GRCh37.p13 chr12: 52,681,800-53,125,929 KRT81, LOC400036, 22 more genes
    nsv6932591copy number variation1nstd229human GRCh38 chr12: 52,648,621-52,659,476 , GRCh37.p13 chr12: 53,042,405-53,053,260 KRT2
    nsv6931489copy number variation1nstd229human GRCh38 chr12: 52,539,483-53,033,896 , GRCh37.p13 chr12: 52,933,267-53,427,680 ARL2BPP2, KRT4, 23 more genes
    nsv6637301copy number variation1nstd102humanUncertain significance GRCh37 chr12: 52,914,324-53,250,644 , GRCh38.p12 chr12: 52,520,540-52,856,860 KRT126P, KRT5, 19 more genes
    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
    nsv6463611copy number variation1nstd223human GRCh38 chr12: 52,643,767-52,644,319 , GRCh37.p13 chr12: 53,037,551-53,038,103 KRT2
    nsv6462201copy number variation1nstd223human GRCh38 chr12: 52,520,433-52,849,892 , GRCh37.p13 chr12: 52,914,217-53,243,676 KRT1, ARL2BPP2, 19 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
    nsv5946724copy number variation1nstd209human GRCh38 chr12: 52,646,092-52,659,840 , GRCh37.p13 chr12: 53,039,876-53,053,624 KRT2
    nsv5855377copy number variation1nstd209human GRCh38 chr12: 52,647,344-52,650,900 , GRCh37.p13 chr12: 53,041,128-53,044,684 KRT2
    nsv5853259copy number variation1nstd209human GRCh38 chr12: 52,646,994-52,658,176 , GRCh37.p13 chr12: 53,040,778-53,051,960 KRT2
    nsv5850650copy number variation1nstd209human GRCh38 chr12: 52,650,901-52,655,726 , GRCh37.p13 chr12: 53,044,685-53,049,510 KRT2
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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