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Items: 1 to 20 of 104

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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
    nsv6921573copy number variation1nstd229human GRCh38 chr12: 55,436,272-55,647,452 , GRCh37.p13 chr12: 55,830,056-56,041,236 LOC100418940, OR2AP1, 8 more genes
    nsv6465149copy number variation1nstd223human GRCh38 chr12: 55,404,985-55,664,522 , GRCh37.p13 chr12: 55,798,769-56,058,306 OR6C2, OR6C70, 11 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
    nsv5506097copy number variation1nstd206human GRCh38 chr12: 55,493,627-55,509,776 , GRCh37.p13 chr12: 55,887,411-55,903,560 OR6C68
    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
    nsv4972833copy number variation1nstd200human GRCh38 chr12: 55,490,630-55,490,704 , GRCh37.p13 chr12: 55,884,414-55,884,488 OR6C68
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4837389copy number variation1nstd200human GRCh37 chr12: 55,884,414-55,884,488 , GRCh38.p12 chr12: 55,490,630-55,490,704 OR6C68
    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
    nsv4200458copy number variation1nstd166human GRCh37.p13 chr12: 55,884,000-55,897,000 , GRCh38.p12 chr12: 55,490,216-55,503,216 OR6C68
    nsv3966325copy number variation1nstd168human GRCh38 chr12: 55,485,543-55,540,091 , GRCh37.p13 chr12: 55,879,327-55,933,875 OR6C68, OR6C64P
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