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 253

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7065985inversion1nstd229human GRCh38 chr20: 63,509,212-64,282,670 , GRCh37.p13 chr20: 62,140,565-62,914,023 RNU1-134P, MIR6813, 46 more genes
    nsv7065815inversion1nstd229human GRCh38 chr20: 63,885,126-63,887,452 , GRCh37.p13 chr20: 62,516,479-62,518,805 TPD52L2
    nsv7061289inversion1nstd229human GRCh38 chr20: 63,026,492-64,008,482 , GRCh37.p13 chr20: 61,657,844-62,639,835 TNFRSF6B, MIR941-5, 60 more genes
    nsv7061138inversion1nstd229human GRCh38 chr20: 63,884,839-63,891,047 , GRCh37.p13 chr20: 62,516,192-62,522,400 TPD52L2
    nsv7059476inversion1nstd229human GRCh38 chr20: 63,024,183-64,005,567 , GRCh37.p13 chr20: 61,655,535-62,636,920 RTEL1-TNFRSF6B, LOC105372721, 60 more genes
    nsv7028864copy number variation1nstd229human GRCh38 chr20: 63,770,901-63,920,600 , GRCh37.p13 chr20: 62,402,254-62,551,953 DNAJC5, C20orf181, 11 more genes
    nsv7028157copy number variation1nstd229human GRCh38 chr20: 63,871,366-63,875,975 , GRCh37.p13 chr20: 62,502,719-62,507,328 TPD52L2
    nsv7027026copy number variation1nstd229human GRCh38 chr20: 63,882,924-63,972,300 , GRCh37.p13 chr20: 62,514,277-62,603,653 MIR941-1, MIR941-3, 12 more genes
    nsv7025635copy number variation1nstd229human GRCh38 chr20: 63,862,501-63,878,000 , GRCh37.p13 chr20: 62,493,854-62,509,353 LOC112268269, ABHD16B, 1 more genes
    nsv7024078copy number variation1nstd229human GRCh38 chr20: 63,862,721-63,867,235 , GRCh37.p13 chr20: 62,494,074-62,498,588 ABHD16B, TPD52L2, 1 more genes
    nsv7023427copy number variation1nstd229human GRCh38 chr20: 63,849,356-63,872,736 , GRCh37.p13 chr20: 62,480,709-62,504,089 LOC112268269, ABHD16B, 1 more genes
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6598525inversion1nstd223human GRCh38 chr20: 63,626,801-63,956,899 , GRCh37.p13 chr20: 62,258,154-62,588,252 SLC2A4RG, ABHD16B, 26 more genes
    nsv6547428copy number variation1nstd223human GRCh38 chr20: 63,864,082-63,864,443 , GRCh37.p13 chr20: 62,495,435-62,495,796 LOC112268269, TPD52L2
    nsv6538776copy number variation1nstd223human GRCh38 chr20: 63,886,600-63,886,894 , GRCh37.p13 chr20: 62,517,953-62,518,247 TPD52L2
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 HAR1A, PPDPF, 100 more genes
    nsv6314091copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202 TPD52L2, MIR941-5, 72 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