U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 21

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4675025copy number variation1nstd102humanUncertain significance GRCh37 chr15: 63,555,363-63,800,908 , GRCh38.p12 chr15: 63,263,164-63,508,709 USP3, CA12, 3 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 USP3, H3P40, 1616 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 USP3, RNU6-18P, 1442 more genes
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 USP3, C2CD4A, 40 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 USP3, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 USP3, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 USP3, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 USP3, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 USP3, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 USP3, RNU6-953P, 1385 more genes
    nsv3899559copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595 USP3, CILP, 1176 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 USP3, GAPDHP61, 840 more genes
    nsv3883273copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 63,414,894-66,439,797 , GRCh38.p12 chr15: 63,122,695-66,147,459 USP3, CA12, 66 more genes
    nsv3905308copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 59,297,293-102,480,888 , GRCh38.p12 chr15: 59,005,094-101,940,685 USP3, ACAN, 861 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 USP3, SNRPCP18, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 USP3, SNORD116-23, 1622 more genes
    nsv3911945copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 USP3, HDDC3, 1622 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 USP3, RPL21P113, 1428 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 USP3, GCHFR, 1382 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 USP3, LOC105370794, 1173 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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