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 163

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5621482insertion1nstd207human GRCh38 chr1: 160,049,675-160,049,675 , GRCh37.p13 chr1: 160,019,465-160,019,465 KCNJ10
    nsv5433015copy number variation1nstd206human GRCh38 chr1: 160,070,221-160,070,285 , GRCh37.p13 chr1: 160,040,011-160,040,075 KCNJ10
    nsv5427730copy number variation1nstd206human GRCh38 chr1: 160,027,536-160,037,873 , GRCh37.p13 chr1: 159,997,326-160,007,663 PIGM, KCNJ10
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5188155mobile element insertion1nstd203human GRCh38 chr1: 160,039,621-160,039,621 , GRCh37.p13 chr1: 160,009,411-160,009,411 KCNJ10
    nsv4903948copy number variation1nstd200human GRCh38 chr1: 159,156,577-160,055,289 , GRCh37.p13 chr1: 159,126,367-160,025,079 , IGSF9, 40 more genes
    nsv4897723copy number variation1nstd200human GRCh38 chr1: 160,066,378-160,066,504 , GRCh37.p13 chr1: 160,036,168-160,036,294 KCNJ10
    nsv4897722copy number variation1nstd200human GRCh38 chr1: 160,027,536-160,037,873 , GRCh37.p13 chr1: 159,997,326-160,007,663 PIGM, KCNJ10
    nsv4784436copy number variation1nstd200human GRCh37 chr1: 159,997,326-160,007,663 , GRCh38.p12 chr1: 160,027,536-160,037,873 KCNJ10, PIGM
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4579405copy number variation1nstd183human GRCh37 chr1: 159,997,324-160,007,663 , GRCh38.p12 chr1: 160,027,534-160,037,873 PIGM, KCNJ10
    nsv4534304insertion1nstd166human GRCh37.p13 chr1: 160,009,396-160,009,396 , GRCh38.p12 chr1: 160,039,606-160,039,606 KCNJ10
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4450321copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,808,188-161,011,163 , GRCh38.p12 chr1: 159,838,398-161,041,373 LOC107985216, PPIAP37, 50 more genes
    nsv4393349copy number variation1nstd174human GRCh37 chr1: 159,997,324-160,010,151 , GRCh38.p12 chr1: 160,027,534-160,040,361 KCNJ10, PIGM
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4069977copy number variation1nstd166human GRCh37.p13 chr1: 159,997,326-160,007,663 , GRCh38.p12 chr1: 160,027,536-160,037,873 KCNJ10, PIGM
    nsv3966364copy number variation1nstd168human GRCh38 chr1: 159,996,477-160,063,016 , GRCh37.p13 chr1: 159,966,267-160,032,806 KCNJ10, RPL27AP2, 1 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 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