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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980312insertion1nstd209human GRCh38 chr12: 52,752,210-52,752,210 , GRCh37.p13 chr12: 53,145,994-53,145,994 KRT127P
    nsv5663752insertion1nstd207human GRCh38 chr12: 52,752,210-52,752,210 , GRCh37.p13 chr12: 53,145,994-53,145,994 KRT127P
    nsv5544468insertion1nstd206human GRCh38 chr12: 52,752,226-52,752,247 , GRCh37.p13 chr12: 53,146,010-53,146,031 KRT127P
    nsv5140012mobile element insertion1nstd203human GRCh38 chr12: 52,752,217-52,752,226 , GRCh37.p13 chr12: 53,146,001-53,146,010 KRT127P
    nsv5138938mobile element insertion1nstd203human GRCh38 chr12: 52,752,215-52,752,226 , GRCh37.p13 chr12: 53,145,999-53,146,010 KRT127P
    nsv5134532mobile element insertion1nstd203human GRCh38 chr12: 52,752,210-52,752,226 , GRCh37.p13 chr12: 53,145,994-53,146,010 KRT127P
    nsv5127252mobile element insertion1nstd203human GRCh38 chr12: 52,752,383-52,752,406 , GRCh37.p13 chr12: 53,146,167-53,146,190 KRT127P
    nsv5121057mobile element insertion1nstd203human GRCh38 chr12: 52,752,406-52,752,427 , GRCh37.p13 chr12: 53,146,190-53,146,211 KRT127P
    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
    nsv4972726copy number variation1nstd200human GRCh38 chr12: 52,749,161-52,753,096 , GRCh37.p13 chr12: 53,142,945-53,146,880 KRT127P, BTBD10P1
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4830357copy number variation1nstd200human GRCh37 chr12: 53,142,945-53,146,880 , GRCh38.p12 chr12: 52,749,161-52,753,096 KRT127P, BTBD10P1
    nsv4760006insertion1nstd199human GRCh37 chr12: 53,146,003-53,146,003 , GRCh38.p12 chr12: 52,752,219-52,752,219 KRT127P
    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
    nsv4719739insertion1nstd186human GRCh37 chr12: 53,145,994-53,145,994 , GRCh38.p12 chr12: 52,752,210-52,752,210 KRT127P
    nsv4675782copy number variation1nstd102humanUncertain significance GRCh37 chr12: 52,914,323-53,238,344 , GRCh38.p12 chr12: 52,520,539-52,844,560 KRT5, KRT2, 19 more genes
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 , EIF4B, 163 more genes
    nsv4545274insertion1nstd166human GRCh37.p13 chr12: 53,145,994-53,145,994 , GRCh38.p12 chr12: 52,752,210-52,752,210 KRT127P
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