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 161

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6996893copy number variation1nstd229human GRCh38 chr17: 35,782,277-35,795,005 , GRCh37.p13 chr17|NW_004166864.2: 74,445-87,173 MMP28
    nsv6994603copy number variation1nstd229human GRCh38 chr17: 35,768,310-35,773,294 , GRCh37.p13 chr17|NW_004166864.2: 60,478-65,462 MMP28
    nsv6990049copy number variation1nstd229human GRCh38 chr17: 35,777,302-35,779,904 , GRCh37.p13 chr17|NW_004166864.2: 69,470-72,072 MMP28
    nsv6984326copy number variation1nstd229human GRCh38 chr17: 35,761,744-35,765,833 , GRCh37.p13 chr17: 34,088,763-34,092,487 , GRCh37.p13 chr17|NW_004166864.2: 53,912-58,001 MMP28, C17orf50
    nsv6978351copy number variation1nstd229human GRCh38 chr17: 35,781,768-35,785,287 , GRCh37.p13 chr17|NW_004166864.2: 73,936-77,455 MMP28
    nsv6590300inversion1nstd223human GRCh38 chr17: 35,783,076-35,784,266 , GRCh37.p13 chr17|NW_004166864.2: 75,244-76,434 MMP28
    nsv6578993inversion1nstd223human GRCh38 chr17: 35,756,485-35,757,037 , GRCh37.p13 chr17|NW_004166864.2: 48,653-49,205 , GRCh37.p13 chr17: 34,083,504-34,084,056 MMP28
    nsv6504067copy number variation1nstd223human GRCh38 chr17: 35,785,984-35,797,861 , GRCh37.p13 chr17|NW_004166864.2: 78,152-90,029 MMP28
    nsv6498234copy number variation1nstd223human GRCh38 chr17: 35,757,407-35,761,855 , GRCh37.p13 chr17: 34,084,426-34,088,874 , GRCh37.p13 chr17|NW_004166864.2: 49,575-54,023 MMP28, C17orf50
    nsv6250761mobile element insertion1nstd215human GRCh38 chr17: 35,771,752-35,771,752 , GRCh37.p13 chr17|NW_004166864.2: 63,920-63,920 MMP28
    nsv6133353copy number variation1nstd213human GRCh37 chr17: 33,210,000-34,670,001 , GRCh38.p12 chr17: 34,882,981-35,919,248 AP2B1, E2F3P1, 48 more genes
    nsv6133052copy number variation1nstd213human GRCh37 chr17: 33,850,000-34,430,001 , GRCh38.p12 chr17: 35,522,981-35,919,248 RASL10B, RDM1, 21 more genes
    nsv6133050copy number variation1nstd213human GRCh37 chr17: 32,790,000-34,510,001 , GRCh38.p12 chr17: 34,462,981-35,919,248 AP2B1, E2F3P1, 53 more genes
    nsv6024460copy number variation1nstd212human GRCh38 chr17: 35,793,990-35,794,048 , GRCh37.p13 chr17|NW_004166864.2: 86,158-86,216 MMP28
    nsv5972965insertion1nstd209human GRCh38 chr17: 35,786,699-35,786,699 , GRCh37.p13 chr17|NW_004166864.2: 78,867-78,867 MMP28
    nsv5938271copy number variation1nstd209human GRCh38 chr17: 35,793,981-35,794,095 , GRCh37.p13 chr17|NW_004166864.2: 86,149-86,263 MMP28
    nsv5720768mobile element insertion2nstd211human GRCh38 chr17: 35,757,776-35,757,776 , GRCh37.p13 chr17|NW_004166864.2: 49,944-49,944 , GRCh37.p13 chr17: 34,084,795-34,084,795 , MMP28
    nsv5707733mobile element insertion1nstd211human GRCh38 chr17: 35,786,715-35,786,715 , GRCh37.p13 chr17|NW_004166864.2: 78,883-78,883 MMP28
    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