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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966333insertion1nstd209human GRCh38 chr2: 47,245,957-47,245,957 , GRCh37.p13 chr2: 47,473,096-47,473,096 EPCAM-DT
    nsv5885885copy number variation1nstd209human GRCh38 chr2: 47,255,691-47,255,747 , GRCh37.p13 chr2: 47,482,830-47,482,886 LOC107985882, EPCAM-DT
    nsv5884534copy number variation1nstd209human GRCh38 chr2: 47,282,999-47,284,328 , GRCh37.p13 chr2: 47,510,138-47,511,467 EPCAM-DT
    nsv5879558copy number variation1nstd209human GRCh38 chr2: 47,290,101-47,290,711 , GRCh37.p13 chr2: 47,517,240-47,517,850 EPCAM-DT
    nsv5877567copy number variation1nstd209human GRCh38 chr2: 47,197,964-47,198,094 , GRCh37.p13 chr2: 47,425,103-47,425,233 EPCAM-DT
    nsv5870626copy number variation1nstd209human GRCh38 chr2: 47,317,784-47,318,159 , GRCh37.p13 chr2: 47,544,923-47,545,298 EPCAM-DT
    nsv5869753copy number variation1nstd209human GRCh38 chr2: 47,341,423-47,345,522 , GRCh37.p13 chr2: 47,568,562-47,572,661 EPCAM-DT
    nsv5833364copy number variation1nstd209human GRCh38 chr2: 47,341,389-47,345,562 , GRCh37.p13 chr2: 47,568,528-47,572,701 EPCAM-DT
    nsv5832686copy number variation1nstd209human GRCh38 chr2: 47,282,964-47,284,363 , GRCh37.p13 chr2: 47,510,103-47,511,502 EPCAM-DT
    nsv5715513mobile element insertion1nstd211human GRCh38 chr2: 47,299,110-47,299,110 , GRCh37.p13 chr2: 47,526,249-47,526,249 EPCAM-DT
    nsv5679241mobile element insertion1nstd211human GRCh38 chr2: 47,313,966-47,313,966 , GRCh37.p13 chr2: 47,541,105-47,541,105 EPCAM-DT
    nsv5622161insertion1nstd207human GRCh38 chr2: 47,255,882-47,255,882 , GRCh37.p13 chr2: 47,483,021-47,483,021 LOC107985882, EPCAM-DT
    nsv5573703copy number variation1nstd207human GRCh38 chr2: 47,255,828-47,255,879 , GRCh37.p13 chr2: 47,482,967-47,483,018 LOC107985882, EPCAM-DT
    nsv5572557copy number variation1nstd207human GRCh38 chr2: 47,245,944-47,245,997 , GRCh37.p13 chr2: 47,473,083-47,473,136 EPCAM-DT
    nsv5562634mobile element insertion1nstd206human GRCh38 chr2: 47,299,110-47,299,161 , GRCh37.p13 chr2: 47,526,249-47,526,300 EPCAM-DT
    nsv5554243inversion1nstd206human GRCh38 chr2: 47,276,047-47,288,190 , GRCh37.p13 chr2: 47,503,186-47,515,329 EPCAM-DT
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5538342insertion1nstd206human GRCh38 chr2: 47,288,122-47,288,140 , GRCh37.p13 chr2: 47,515,261-47,515,279 EPCAM-DT
    nsv5453884copy number variation1nstd206human GRCh38 chr2: 47,219,878-47,219,963 , GRCh37.p13 chr2: 47,447,017-47,447,102 LOC105374588, EPCAM-DT
    nsv5453770copy number variation1nstd206human GRCh38 chr2: 47,279,730-47,285,199 , GRCh37.p13 chr2: 47,506,869-47,512,338 EPCAM-DT
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