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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117348mobile element insertion1nstd186human GRCh37 chr12: 70,788,935-70,788,986 , GRCh38.p12 chr12: 70,395,155-70,395,206 KCNMB4
    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
    nsv5970353insertion1nstd209human GRCh38 chr12: 70,395,138-70,395,138 , GRCh37.p13 chr12: 70,788,918-70,788,918 KCNMB4
    nsv5946849copy number variation1nstd209human GRCh38 chr12: 70,384,946-70,384,996 , GRCh37.p13 chr12: 70,778,726-70,778,776 KCNMB4
    nsv5860961copy number variation1nstd209human GRCh38 chr12: 70,396,892-70,398,891 , GRCh37.p13 chr12: 70,790,672-70,792,671 KCNMB4
    nsv5708905mobile element insertion2nstd211human GRCh38 chr12: 70,395,155-70,395,155 , GRCh37.p13 chr12: 70,788,935-70,788,935 KCNMB4
    nsv5648202insertion1nstd207human GRCh38 chr12: 70,395,138-70,395,138 , GRCh37.p13 chr12: 70,788,918-70,788,918 KCNMB4
    nsv5539889insertion1nstd206human GRCh38 chr12: 70,403,589-70,403,589 , GRCh37.p13 chr12: 70,797,369-70,797,369 KCNMB4
    nsv5418055mobile element insertion1nstd206human GRCh38 chr12: 70,395,155-70,395,206 , GRCh37.p13 chr12: 70,788,935-70,788,986 KCNMB4
    nsv5414816mobile element insertion1nstd206human GRCh38 chr12: 70,408,720-70,408,771 , GRCh37.p13 chr12: 70,802,500-70,802,551 KCNMB4
    nsv5369292translocation1nstd200human GRCh38 chr12: 70,366,253-70,366,253 , GRCh38 chr6: 24,550,499-24,550,499 , GRCh37.p13 chr12: 70,760,033-70,760,033 , GRCh37.p13 chr6: 24,550,727-24,550,727 KIAA0319, KCNMB4
    nsv5317216copy number variation1nstd204human GRCh38.p13 chr12: 70,425,352-70,425,979 , GRCh37.p13 chr12: 70,819,132-70,819,759 KCNMB4
    nsv5263214copy number variation1nstd204human GRCh38.p13 chr12: 70,365,849-70,367,027 , GRCh37.p13 chr12: 70,759,629-70,760,807 KCNMB4
    nsv5139312mobile element insertion1nstd203human GRCh38 chr12: 70,395,138-70,395,155 , GRCh37.p13 chr12: 70,788,918-70,788,935 KCNMB4
    nsv5132016mobile element insertion1nstd203human GRCh38 chr12: 70,395,144-70,395,155 , GRCh37.p13 chr12: 70,788,924-70,788,935 KCNMB4
    nsv5124395mobile element insertion1nstd203human GRCh38 chr12: 70,395,145-70,395,155 , GRCh37.p13 chr12: 70,788,925-70,788,935 KCNMB4
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 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
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