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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv6937754copy number variation1nstd229human GRCh38 chr12: 52,777,005-52,808,702 , GRCh37.p13 chr12: 53,170,789-53,202,486 KRT76, KRT3, 1 more genes
    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
    nsv6929676copy number variation1nstd229human GRCh38 chr12: 52,810,688-52,815,019 , GRCh37.p13 chr12: 53,204,472-53,208,803 KRT4
    nsv6928480copy number variation1nstd229human GRCh38 chr12: 52,805,571-52,806,176 , GRCh37.p13 chr12: 53,199,355-53,199,960 KRT3, KRT4
    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
    nsv6470077copy number variation1nstd223human GRCh38 chr12: 52,805,571-52,806,176 , GRCh37.p13 chr12: 53,199,355-53,199,960 KRT4, KRT3
    nsv6464949copy number variation1nstd223human GRCh38 chr12: 52,791,200-52,807,638 , GRCh37.p13 chr12: 53,184,984-53,201,422 KRT3, KRT4
    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
    nsv5700259mobile element insertion1nstd211human GRCh38 chr12: 52,804,884-52,804,884 , GRCh37.p13 chr12: 53,198,668-53,198,668 KRT3, KRT4
    nsv5427440mobile element insertion1nstd206human GRCh38 chr12: 52,804,884-52,804,935 , GRCh37.p13 chr12: 53,198,668-53,198,719 KRT4, KRT3
    nsv5130436mobile element insertion1nstd203human GRCh38 chr12: 52,805,771-52,805,788 , GRCh37.p13 chr12: 53,199,555-53,199,572 KRT3, KRT4
    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
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
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