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Items: 1 to 20 of 437

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6627164copy number variation1nstd224human GRCh37 chr21: 47,558,994-47,585,817 , GRCh38.p12 chr21: 46,139,080-46,165,903 , GRCh38.p12 chr21|NT_187626.1: 1-25,346 FTCD-AS1, FTCD, 1 more genes
    nsv6627025copy number variation1nstd224human GRCh37 chr21: 47,558,528-47,588,465 , GRCh38.p12 chr21: 46,138,614-46,168,551 , GRCh38.p12 chr21|NT_187626.1: 1-27,994 SPATC1L, FTCD-AS1, 1 more genes
    nsv6626887copy number variation2nstd224human GRCh37 chr21: 47,565,371-47,588,465 , GRCh38.p12 chr21: 46,145,457-46,168,551 , GRCh38.p12 chr21|NT_187626.1: 4,516-27,994 SPATC1L, FTCD, 1 more genes
    nsv6626652copy number variation1nstd224human GRCh37 chr21: 47,552,006-47,666,788 , GRCh38.p12 chr21: 46,132,092-46,246,874 , GRCh38.p12 chr21|NT_187626.1: 1-82,692 COL6A2, LSS, 6 more genes
    nsv6311116copy number variation1nstd102humanUncertain significance GRCh37 chr21: 47,531,391-47,666,820 , GRCh38.p12 chr21: 46,111,477-46,246,906 , GRCh38.p12 chr21|NT_187626.1: 1-82,692 MCM3AP-AS1, FTCD-AS1, 6 more genes
    nsv6306188copy number variation1nstd186human GRCh37 chr21: 47,590,091-47,590,703 , GRCh38.p12 chr21: 46,170,177-46,170,789 , GRCh38.p12 chr21|NT_187626.1: 31,693-32,158 SPATC1L
    nsv6134089copy number variation1nstd213human GRCh37 chr21: 47,578,879-47,705,228 , GRCh38.p12 chr21: 46,158,965-46,285,314 , GRCh38.p12 chr21|NT_187626.1: 18,028-82,692 LSS, MCM3AP, 4 more genes
    nsv6130668insertion1nstd186human GRCh37 chr21: 47,580,928-47,580,944 , GRCh38.p12 chr21: 46,161,014-46,161,030 , GRCh38.p12 chr21|NT_187626.1: 20,077-20,093 SPATC1L
    nsv6128682copy number variation1nstd186human GRCh37 chr21: 47,603,538-47,603,818 , GRCh38.p12 chr21: 46,183,624-46,183,904 , GRCh38.p12 chr21|NT_187626.1: 44,994-45,274 SPATC1L
    nsv6126353copy number variation1nstd186human GRCh37 chr21: 47,590,461-47,590,763 , GRCh38.p12 chr21: 46,170,547-46,170,849 , GRCh38.p12 chr21|NT_187626.1: 31,916-32,218 SPATC1L
    nsv6112961copy number variation1nstd186human GRCh37 chr21: 47,589,248-47,590,959 , GRCh38.p12 chr21: 46,169,334-46,171,045 , GRCh38.p12 chr21|NT_187626.1: 28,777-32,414 SPATC1L
    nsv5393417copy number variation1nstd186human GRCh37 chr21: 47,603,522-47,603,739 , GRCh38.p12 chr21|NT_187626.1: 44,978-45,195 , GRCh38.p12 chr21: 46,183,608-46,183,825 SPATC1L
    nsv5392660copy number variation1nstd186human GRCh37 chr21: 47,590,631-47,590,844 , GRCh38.p12 chr21|NT_187626.1: 32,086-32,299 , GRCh38.p12 chr21: 46,170,717-46,170,930 SPATC1L
    nsv5389662copy number variation1nstd186human GRCh37 chr21: 47,603,434-47,603,872 , GRCh38.p12 chr21: 46,183,520-46,183,958 , GRCh38.p12 chr21|NT_187626.1: 44,890-45,328 SPATC1L
    nsv4880230inversion1nstd200human GRCh37 chr21: 47,605,758-47,607,000 , GRCh38.p12 chr21: 46,185,844-46,187,086 , GRCh38.p12 chr21|NT_187626.1: 47,214-48,456 LSS
    nsv4869316copy number variation1nstd200human GRCh37 chr21: 47,556,268-47,572,582 , GRCh38.p12 chr21|NT_187626.1: 1-11,727 , GRCh38.p12 chr21: 46,136,354-46,152,668 FTCD-AS1, FTCD
    nsv4863521copy number variation1nstd200human GRCh37 chr21: 47,638,156-47,640,350 , GRCh38.p12 chr21: 46,218,242-46,220,436 , GRCh38.p12 chr21|NT_187626.1: 79,612-81,806 LSS
    nsv4863520copy number variation1nstd200human GRCh37 chr21: 47,609,742-47,610,876 , GRCh38.p12 chr21|NT_187626.1: 51,198-52,332 , GRCh38.p12 chr21: 46,189,828-46,190,962 LSS
    nsv4863519copy number variation1nstd200human GRCh37 chr21: 47,605,800-47,605,906 , GRCh38.p12 chr21|NT_187626.1: 47,256-47,362 , GRCh38.p12 chr21: 46,185,886-46,185,992 0
    nsv4863518copy number variation1nstd200human GRCh37 chr21: 47,603,520-47,603,741 , GRCh38.p12 chr21: 46,183,606-46,183,827 , GRCh38.p12 chr21|NT_187626.1: 44,976-45,197 SPATC1L
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