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 172

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977229insertion1nstd209human GRCh38 chr15: 89,479,122-89,479,122 , GRCh37.p13 chr15: 90,022,353-90,022,353 RHCG
    nsv5939741copy number variation1nstd209human GRCh38 chr15: 89,470,539-89,522,530 , GRCh37.p13 chr15: 90,013,770-90,065,761 LINC00928, RHCG
    nsv5880877copy number variation1nstd209human GRCh38 chr15: 89,464,570-89,489,792 , GRCh37.p13 chr15: 90,007,801-90,033,023 RHCG, LOC105370964, 1 more genes
    nsv5872786copy number variation1nstd209human GRCh38 chr15: 89,477,429-89,522,528 , GRCh37.p13 chr15: 90,020,660-90,065,759 RHCG, LINC00928
    nsv5661583insertion1nstd207human GRCh38 chr15: 89,479,122-89,479,122 , GRCh37.p13 chr15: 90,022,353-90,022,353 RHCG
    nsv5651953insertion1nstd207human GRCh38 chr15: 89,474,828-89,474,828 , GRCh37.p13 chr15: 90,018,059-90,018,059 RHCG
    nsv5586297copy number variation1nstd207human GRCh38 chr15: 89,474,906-89,474,990 , GRCh37.p13 chr15: 90,018,137-90,018,221 RHCG
    nsv5557822sequence alteration1nstd206human GRCh38 chr15: 89,475,927-89,475,939 , GRCh37.p13 chr15: 90,019,158-90,019,170 RHCG
    nsv5528106copy number variation1nstd206human GRCh38 chr15: 89,496,767-89,497,463 , GRCh37.p13 chr15: 90,039,998-90,040,694 RHCG
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4746579copy number variation1nstd199human GRCh37 chr15: 90,018,047-90,018,100 , GRCh38.p12 chr15: 89,474,816-89,474,869 RHCG
    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
    nsv4724428insertion1nstd186human GRCh37 chr15: 90,022,332-90,022,332 , GRCh38.p12 chr15: 89,479,101-89,479,101 RHCG
    nsv4679244copy number variation1nstd189human GRCh37.p13 chr15: 89,903,203-90,447,762 , GRCh38.p12 chr15: 89,359,972-89,904,530 , ANPEP, 26 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
    nsv4626753copy number variation1nstd183human GRCh37 chr15: 89,684,517-90,163,339 , GRCh38.p12 chr15: 89,141,286-89,620,108 , ABHD2, 14 more genes
    nsv4552877insertion1nstd166human GRCh37.p13 chr15: 90,022,332-90,022,332 , GRCh38.p12 chr15: 89,479,101-89,479,101 RHCG
    nsv4552855insertion1nstd166human GRCh37.p13 chr15: 90,013,233-90,013,233 , GRCh38.p12 chr15: 89,470,002-89,470,002 RHCG, LOC112268153
    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
    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
    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