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Items: 1 to 20 of 167

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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
    nsv7073215inversion1nstd229human GRCh38 chr12: 53,216,605-53,219,713 , GRCh37.p13 chr12: 53,610,389-53,613,497 RARG
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv6930060copy number variation1nstd229human GRCh38 chr12: 53,216,366-53,219,009 , GRCh37.p13 chr12: 53,610,150-53,612,793 RARG
    nsv6929806copy number variation1nstd229human GRCh38 chr12: 53,210,931-53,211,032 , GRCh37.p13 chr12: 53,604,715-53,604,816 RARG
    nsv6928394copy number variation1nstd229human GRCh38 chr12: 53,230,937-53,231,133 , GRCh37.p13 chr12: 53,624,721-53,624,917 RARG
    nsv6925991copy number variation1nstd229human GRCh38 chr12: 53,215,794-53,227,361 , GRCh37.p13 chr12: 53,609,578-53,621,145 RARG
    nsv6307507copy number variation1nstd186human GRCh37 chr12: 53,604,715-53,604,821 , GRCh38.p12 chr12: 53,210,931-53,211,037 RARG
    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
    nsv5659903insertion1nstd207human GRCh38 chr12: 53,226,289-53,226,289 , GRCh37.p13 chr12: 53,620,073-53,620,073 RARG
    nsv5494563copy number variation1nstd206human GRCh38 chr12: 53,210,931-53,211,037 , GRCh37.p13 chr12: 53,604,715-53,604,821 RARG
    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
    nsv4836760copy number variation1nstd200human GRCh37 chr12: 53,603,607-53,604,000 , GRCh38.p12 chr12: 53,209,823-53,210,216 RARG
    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
    nsv4729204copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 53,614,278-53,971,802 , GRCh38.p12 chr12: 53,220,494-53,578,018 AMHR2, PCBP2, 18 more genes
    nsv4729090copy number variation1nstd102humanUncertain significance GRCh37 chr12: 53,372,321-53,864,490 , GRCh38.p12 chr12: 52,978,537-53,470,706 SPRYD3, ITGB7, 25 more genes
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