U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 90

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917921copy number variation1nstd229human GRCh38 chr11: 6,318,131-6,319,985 , GRCh37.p13 chr11: 6,339,361-6,341,215 CAVIN3, LOC101927825
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6915106copy number variation1nstd229human GRCh38 chr11: 6,247,901-6,382,100 , GRCh37.p13 chr11: 6,269,131-6,403,330 LOC101927825, CAVIN3, 1 more genes
    nsv6912187copy number variation1nstd229human GRCh38 chr11: 6,293,185-6,374,864 , GRCh37.p13 chr11: 6,314,415-6,396,094 LOC101927825, CAVIN3
    nsv6911748copy number variation1nstd229human GRCh38 chr11: 6,314,301-6,441,800 , GRCh37.p13 chr11: 6,335,531-6,463,030 HPX, CAVIN3, 3 more genes
    nsv6910065copy number variation1nstd229human GRCh38 chr11: 6,320,321-6,339,245 , GRCh37.p13 chr11: 6,341,551-6,360,475 LOC101927825, CAVIN3
    nsv6900827copy number variation1nstd229human GRCh38 chr11: 6,191,411-6,542,996 , GRCh37.p13 chr11: 6,212,641-6,564,226 ARFIP2, RRP8, 14 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6445161copy number variation1nstd223human GRCh38 chr11: 6,320,321-6,339,240 , GRCh37.p13 chr11: 6,341,551-6,360,470 CAVIN3, LOC101927825
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6132268copy number variation1nstd213human GRCh37 chr11: 6,320,000-6,880,001 , GRCh38.p12 chr11: 6,298,770-6,858,770 APBB1, TPP1, 22 more genes
    nsv5505016copy number variation1nstd206human GRCh38 chr11: 6,314,207-6,321,203 , GRCh37.p13 chr11: 6,335,437-6,342,433 LOC101927825, CAVIN3
    nsv5317496copy number variation1nstd204human GRCh37.p13 chr11: 6,341,549-6,360,470 , GRCh38.p13 chr11: 6,320,319-6,339,240 LOC101927825, CAVIN3
    nsv5247028copy number variation1nstd204human GRCh38.p13 chr11: 6,318,601-6,340,800 , GRCh37.p13 chr11: 6,339,831-6,362,030 CAVIN3, LOC101927825
    nsv5242724copy number variation1nstd204human GRCh38.p13 chr11: 6,319,347-6,339,137 , GRCh37.p13 chr11: 6,340,577-6,360,367 CAVIN3, LOC101927825
    nsv4978046copy number variation1nstd200human GRCh38 chr11: 6,320,321-6,339,240 , GRCh37.p13 chr11: 6,341,551-6,360,470 LOC101927825, CAVIN3
    nsv4841792copy number variation1nstd200human GRCh37 chr11: 6,341,551-6,360,470 , GRCh38.p12 chr11: 6,320,321-6,339,240 CAVIN3, LOC101927825
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

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