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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972650inversion1nstd209human GRCh38 chr1: 229,174,728-232,234,598 , GRCh37.p13 chr1: 229,310,475-232,370,344 , ACTA1, 68 more genes
    nsv5971633inversion1nstd209human GRCh38 chr1: 229,416,331-231,831,980 , GRCh37.p13 chr1: 229,552,078-231,967,726 , ACTA1, 56 more genes
    nsv5886557copy number variation1nstd209human GRCh38 chr1: 230,759,694-230,760,193 , GRCh37.p13 chr1: 230,895,440-230,895,939 CAPN9
    nsv5685606mobile element insertion2nstd211human GRCh38 chr1: 230,756,093-230,756,093 , GRCh37.p13 chr1: 230,891,839-230,891,839 CAPN9
    nsv5681135mobile element insertion1nstd211human GRCh38 chr1: 230,770,530-230,770,530 , GRCh37.p13 chr1: 230,906,276-230,906,276 CAPN9
    nsv5445147copy number variation1nstd206human GRCh38 chr1: 230,482,037-231,277,187 , GRCh37.p13 chr1: 230,617,783-231,412,933 , LOC644006, 24 more genes
    nsv5440782copy number variation1nstd206human GRCh38 chr1: 230,781,561-230,783,454 , GRCh37.p13 chr1: 230,917,307-230,919,200 CAPN9, LOC107985359
    nsv5436521copy number variation1nstd206human GRCh38 chr1: 230,759,694-230,760,204 , GRCh37.p13 chr1: 230,895,440-230,895,950 CAPN9
    nsv5434777copy number variation1nstd206human GRCh38 chr1: 230,771,084-230,771,198 , GRCh37.p13 chr1: 230,906,830-230,906,944 CAPN9
    nsv5403077mobile element insertion1nstd206human GRCh38 chr1: 230,756,093-230,756,144 , GRCh37.p13 chr1: 230,891,839-230,891,890 CAPN9
    nsv5400219mobile element insertion1nstd206human GRCh38 chr1: 230,770,530-230,770,581 , GRCh37.p13 chr1: 230,906,276-230,906,327 CAPN9
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5063518mobile element insertion1nstd203human GRCh38 chr1: 230,756,080-230,756,093 , GRCh37.p13 chr1: 230,891,826-230,891,839 CAPN9
    nsv4904449copy number variation1nstd200human GRCh38 chr1: 230,786,979-231,254,882 , GRCh37.p13 chr1: 230,922,725-231,390,628 RNA5SP79, LOC107985359, 15 more genes
    nsv4904446copy number variation1nstd200human GRCh38 chr1: 230,482,037-231,277,187 , GRCh37.p13 chr1: 230,617,783-231,412,933 , GNPAT, 24 more genes
    nsv4899222copy number variation1nstd200human GRCh38 chr1: 230,790,400-230,790,568 , GRCh37.p13 chr1: 230,926,146-230,926,314 CAPN9, LOC107985359
    nsv4899221copy number variation1nstd200human GRCh38 chr1: 230,723,093-230,747,807 , GRCh37.p13 chr1: 230,858,839-230,883,553 CAPN9
    nsv4785245copy number variation1nstd200human GRCh37 chr1: 230,895,440-230,895,950 , GRCh38.p12 chr1: 230,759,694-230,760,204 CAPN9
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
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