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Items: 1 to 20 of 139

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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
    nsv7069071inversion1nstd229human GRCh38 chr12: 53,696,198-53,711,889 , GRCh37.p13 chr12: 54,089,982-54,105,673 CALCOCO1
    nsv7065497inversion1nstd229human GRCh38 chr12: 53,662,246-53,746,941 , GRCh37.p13 chr12: 54,056,030-54,140,725 LOC105369774, ATP5MC2, 1 more genes
    nsv6937354copy number variation1nstd229human GRCh38 chr12: 53,605,001-53,871,600 , GRCh37.p13 chr12: 53,998,785-54,265,384 , ATP5MC2, 8 more genes
    nsv6927293copy number variation1nstd229human GRCh38 chr12: 53,710,423-53,720,528 , GRCh37.p13 chr12: 54,104,207-54,114,312 CALCOCO1
    nsv6474377copy number variation1nstd223human GRCh38 chr12: 53,707,477-53,708,306 , GRCh37.p13 chr12: 54,101,261-54,102,090 CALCOCO1
    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
    nsv6089182insertion1nstd212human GRCh38 chr12: 53,724,188-53,724,188 , GRCh37.p13 chr12: 54,117,972-54,117,972 CALCOCO1
    nsv5976008insertion1nstd209human GRCh38 chr12: 53,724,195-53,724,195 , GRCh37.p13 chr12: 54,117,979-54,117,979 CALCOCO1
    nsv5653523insertion1nstd207human GRCh38 chr12: 53,724,188-53,724,188 , GRCh37.p13 chr12: 54,117,972-54,117,972 CALCOCO1
    nsv5542711insertion1nstd206human GRCh38 chr12: 53,724,194-53,724,194 , GRCh37.p13 chr12: 54,117,978-54,117,978 CALCOCO1
    nsv5136343mobile element insertion1nstd203human GRCh38 chr12: 53,724,188-53,724,194 , GRCh37.p13 chr12: 54,117,972-54,117,978 CALCOCO1
    nsv5135079mobile element insertion1nstd203human GRCh38 chr12: 53,724,181-53,724,194 , GRCh37.p13 chr12: 54,117,965-54,117,978 CALCOCO1
    nsv5132821mobile element insertion1nstd203human GRCh38 chr12: 53,720,388-53,720,401 , GRCh37.p13 chr12: 54,114,172-54,114,185 CALCOCO1
    nsv5124586mobile element insertion1nstd203human GRCh38 chr12: 53,724,180-53,724,194 , GRCh37.p13 chr12: 54,117,964-54,117,978 CALCOCO1
    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
    nsv4985621copy number variation1nstd200human GRCh38 chr12: 53,707,412-53,708,405 , GRCh37.p13 chr12: 54,101,196-54,102,189 CALCOCO1
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