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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5977139insertion1nstd209human GRCh38 chr12: 68,847,160-68,847,160 , GRCh37.p13 chr12: 69,240,940-69,240,940 CPM, MDM2
    nsv5939698copy number variation1nstd209human GRCh38 chr12: 68,826,454-68,826,979 , GRCh37.p13 chr12: 69,220,234-69,220,759 MDM2
    nsv5852681copy number variation1nstd209human GRCh38 chr12: 68,825,103-68,826,302 , GRCh37.p13 chr12: 69,218,883-69,220,082 MDM2
    nsv5647513insertion2nstd207human GRCh38 chr12: 68,833,280-68,833,280 , GRCh37.p13 chr12: 69,227,060-69,227,060 MDM2
    nsv5556951sequence alteration1nstd206human GRCh38 chr12: 68,612,001-69,442,414 , GRCh37.p13 chr12: 69,005,781-69,836,194 , LYZ, 22 more genes
    nsv5318275copy number variation1nstd204human GRCh37.p13 chr12: 69,243,459-69,246,570 , GRCh38.p13 chr12: 68,849,679-68,852,790 CPM, MDM2
    nsv5267589copy number variation1nstd204human GRCh38.p13 chr12: 68,849,575-68,852,813 , GRCh37.p13 chr12: 69,243,355-69,246,593 CPM, MDM2
    nsv5260593copy number variation1nstd204human GRCh38.p13 chr12: 68,830,653-68,834,599 , GRCh37.p13 chr12: 69,224,433-69,228,379 MDM2
    nsv5138812mobile element insertion1nstd203human GRCh38 chr12: 68,834,582-68,834,597 , GRCh37.p13 chr12: 69,228,362-69,228,377 MDM2
    nsv5130922mobile element insertion1nstd203human GRCh38 chr12: 68,807,035-68,807,035 , GRCh37.p13 chr12: 69,200,815-69,200,815 MDM2
    nsv5122526mobile element insertion1nstd203human GRCh38 chr12: 68,847,471-68,847,480 , GRCh37.p13 chr12: 69,241,251-69,241,260 MDM2, CPM
    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
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv5008611copy number variation1nstd200human GRCh38 chr12: 68,844,917-68,848,891 , GRCh37.p13 chr12: 69,238,697-69,242,671 CPM, MDM2
    nsv5008610copy number variation1nstd200human GRCh38 chr12: 68,841,297-68,844,992 , GRCh37.p13 chr12: 69,235,077-69,238,772 MDM2, CPM
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4761901insertion1nstd199human GRCh37 chr12: 69,227,052-69,227,052 , GRCh38.p12 chr12: 68,833,272-68,833,272 MDM2
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