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Items: 1 to 20 of 97

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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
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7068090inversion1nstd229human GRCh38 chr12: 55,153,945-55,601,684 , GRCh37.p13 chr12: 55,547,729-55,995,468 OR6C65, OR6C6, 23 more genes
    nsv6927630copy number variation1nstd229human GRCh38 chr12: 55,400,615-55,417,761 , GRCh37.p13 chr12: 55,794,399-55,811,545 OR6C65, PHC1P1
    nsv6471131copy number variation1nstd223human GRCh38 chr12: 55,316,801-55,434,800 , GRCh37.p13 chr12: 55,710,585-55,828,584 OR6C65, OR6C71P, 8 more genes
    nsv6469930copy number variation1nstd223human GRCh38 chr12: 55,367,501-55,424,000 , GRCh37.p13 chr12: 55,761,285-55,817,784 OR6C73P, OR6C66P, 3 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
    nsv6132597copy number variation1nstd213human GRCh37 chr12: 55,450,000-56,250,001 , GRCh38.p12 chr12: 55,056,216-55,856,217 BLOC1S1, MMP19, 43 more genes
    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
    nsv4985630copy number variation1nstd200human GRCh38 chr12: 55,393,843-55,400,777 , GRCh37.p13 chr12: 55,787,627-55,794,561 OR6C65, OR6C73P
    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
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4207186copy number variation1nstd166human GRCh37.p13 chr12: 55,650,132-56,280,160 , GRCh38.p12 chr12: 55,256,348-55,886,376 PSMB3P1, OR10AE3P, 38 more genes
    nsv3970873insertion1nstd168human GRCh38 chr12: 55,379,894-55,408,842 , GRCh37.p13 chr12: 55,773,678-55,802,626 OR6C65, OR6C66P, 2 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3910529copy number variation1nstd102humanPathogenic NCBI36 chr12: 52,100,657-54,882,993 , GRCh38 chr12: 53,420,606-56,202,942 , GRCh37 chr12: 53,814,390-56,596,726 , OR6C72P, 140 more genes
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