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 477

    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
    nsv7095147copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850 SLC35G3, AP2B1, 26 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
    nsv7069041inversion1nstd229human GRCh38 chr17: 35,623,281-35,624,853 , GRCh37.p13 chr17: 33,950,300-33,951,872 AP2B1
    nsv6997975copy number variation1nstd229human GRCh38 chr17: 35,674,001-35,683,300 , GRCh37.p13 chr17: 34,001,020-34,010,319 AP2B1
    nsv6996414copy number variation1nstd229human GRCh38 chr17: 35,666,883-35,667,088 , GRCh37.p13 chr17: 33,993,902-33,994,107 AP2B1
    nsv6994200copy number variation1nstd229human GRCh38 chr17: 35,679,883-35,682,151 , GRCh37.p13 chr17: 34,006,902-34,009,170 AP2B1
    nsv6982202copy number variation1nstd229human GRCh38 chr17: 34,998,758-35,727,529 , GRCh37.p13 chr17: 33,325,777-34,034,851 SLFN11, LOC105371932, 32 more genes
    nsv6982095copy number variation1nstd229human GRCh38 chr17: 35,625,078-35,625,977 , GRCh37.p13 chr17: 33,952,097-33,952,996 AP2B1
    nsv6981206copy number variation1nstd229human GRCh38 chr17: 35,703,281-35,704,926 , GRCh37.p13 chr17: 34,030,300-34,031,945 AP2B1
    nsv6980979copy number variation1nstd229human GRCh38 chr17: 35,631,147-35,631,209 , GRCh37.p13 chr17: 33,958,166-33,958,228 AP2B1
    nsv6634448copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,756,756-34,005,513 , GRCh38.p12 chr17: 35,429,737-35,678,494 LOC100420062, TAF5LP1, 13 more genes
    nsv6588068inversion1nstd223human GRCh38 chr17: 35,694,911-35,695,940 , GRCh37.p13 chr17: 34,021,930-34,022,959 AP2B1
    nsv6587643inversion1nstd223human GRCh38 chr17: 35,638,491-35,640,236 , GRCh37.p13 chr17: 33,965,510-33,967,255 AP2B1
    nsv6586737inversion1nstd223human GRCh38 chr17: 35,623,281-35,624,853 , GRCh37.p13 chr17: 33,950,300-33,951,872 AP2B1
    nsv6585625inversion1nstd223human GRCh38 chr17: 35,648,319-35,649,488 , GRCh37.p13 chr17: 33,975,338-33,976,507 AP2B1
    nsv6584486inversion1nstd223human GRCh38 chr17: 35,599,673-35,600,140 , GRCh37.p13 chr17: 33,926,692-33,927,159 AP2B1
    nsv6583047inversion1nstd223human GRCh38 chr17: 35,637,710-35,638,783 , GRCh37.p13 chr17: 33,964,729-33,965,802 AP2B1
    nsv6579555inversion1nstd223human GRCh38 chr17: 35,695,099-35,695,811 , GRCh37.p13 chr17: 34,022,118-34,022,830 AP2B1
    nsv6579302inversion1nstd223human GRCh38 chr17: 35,686,032-35,686,856 , GRCh37.p13 chr17: 34,013,051-34,013,875 AP2B1
    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