U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 430

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4863517copy number variation1nstd200human 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
    nsv4863516copy number variation1nstd200human GRCh37 chr21: 47,570,237-47,592,762 , GRCh38.p12 chr21: 46,150,323-46,172,848 , GRCh38.p12 chr21|NT_187626.1: 9,382-34,218 SPATC1L, FTCD, 1 more genes
    nsv4863515copy number variation1nstd200human GRCh37 chr21: 47,565,710-47,565,762 , GRCh38.p12 chr21|NT_187626.1: 4,855-4,907 , GRCh38.p12 chr21: 46,145,796-46,145,848 FTCD
    nsv4756834insertion1nstd199human GRCh37 chr21: 47,564,276-47,564,276 , GRCh38.p12 chr21: 46,144,362-46,144,362 , GRCh38.p12 chr21|NT_187626.1: 3,421-3,421 FTCD
    nsv4754987insertion1nstd199human GRCh37 chr21: 47,565,628-47,565,628 , GRCh38.p12 chr21: 46,145,714-46,145,714 , GRCh38.p12 chr21|NT_187626.1: 4,773-4,773 FTCD
    nsv4753585insertion1nstd199human GRCh37 chr21: 47,580,910-47,580,910 , GRCh38.p12 chr21|NT_187626.1: 20,059-20,059 , GRCh38.p12 chr21: 46,160,996-46,160,996 SPATC1L
    nsv4746853copy number variation1nstd199human GRCh37 chr21: 47,622,052-47,622,189 , GRCh38.p12 chr21: 46,202,138-46,202,275 , GRCh38.p12 chr21|NT_187626.1: 63,508-63,645 LSS
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center