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 155

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380768copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,290,623-91,512,067 , GRCh38.p12 chr15: 90,747,393-90,968,837 BLM, MAN2A2, 9 more genes
    nsv5152928mobile element insertion1nstd203human GRCh38 chr15: 90,883,984-90,883,994 , GRCh37.p13 chr15: 91,427,214-91,427,224 FES
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4681314copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,326,042-91,512,067 , GRCh38.p12 chr15: 90,782,812-90,968,837 MAN2A2, UNC45A, 9 more genes
    nsv4675917copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,347,599-91,491,931 , GRCh38.p12 chr15: 90,804,369-90,948,701 FES, MAN2A2, 6 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4457347copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,276,782-91,550,953 , GRCh38.p12 chr15: 90,733,551-91,007,723 BLM, MAN2A2, 10 more genes
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4385824copy number variation1nstd173human GRCh37 chr15: 90,250,919-91,461,024 , GRCh38.p12 chr15: 89,707,688-90,917,794 , LOC100631255, 44 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4375224copy number variation1nstd173human GRCh37 chr15: 90,246,823-91,461,537 , GRCh38.p12 chr15: 89,703,592-90,918,307 , RNU6-1111P, 44 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
    nsv3920248copy number variation1nstd102humanPathogenic NCBI36 chr15: 87,618,716-100,262,146 , GRCh37.p13 chr15: 89,817,712-102,444,623 , GRCh38.p12 chr15: 89,274,481-101,904,420 FAM149B1P1, MIR9-3HG, 229 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919393copy number variation1nstd102humanPathogenic NCBI36 chr15: 84,170,900-100,278,724 , GRCh37 chr15: 86,369,896-102,461,201 , GRCh38 chr15: 85,826,665-101,920,998 LOC105370997, LOC102724465, 270 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    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