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 184

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130721insertion1nstd186human GRCh37 chr17: 16,248,725-16,248,725 , GRCh38.p12 chr17: 16,345,411-16,345,411 PIGL, CENPV
    nsv6127083copy number variation1nstd186human GRCh37 chr17: 16,248,589-16,248,725 , GRCh38.p12 chr17: 16,345,275-16,345,411 CENPV, PIGL
    nsv5980264insertion1nstd209human GRCh38 chr17: 16,353,372-16,353,372 , GRCh37.p13 chr17: 16,256,686-16,256,686 CENPV
    nsv5977405insertion1nstd209human GRCh38 chr17: 16,345,411-16,345,411 , GRCh37.p13 chr17: 16,248,725-16,248,725 PIGL, CENPV
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5945891copy number variation1nstd209human GRCh38 chr17: 15,750,946-16,668,217 , GRCh37.p13 chr17: 15,654,260-16,571,531 ADORA2B, MIR1288, 34 more genes
    nsv5943631copy number variation1nstd209human GRCh38 chr17: 15,758,933-16,863,323 , GRCh37.p13 chr17: 15,662,247-16,766,637 , MIR1288, 50 more genes
    nsv5940764copy number variation1nstd209human GRCh38 chr17: 15,758,291-16,862,696 , GRCh37.p13 chr17: 15,661,605-16,766,010 , ZSWIM5P1, 50 more genes
    nsv5657435insertion1nstd207human GRCh38 chr17: 16,345,411-16,345,411 , GRCh37.p13 chr17: 16,248,725-16,248,725 PIGL, CENPV
    nsv5553347insertion1nstd206human GRCh38 chr17: 16,353,380-16,353,400 , GRCh37.p13 chr17: 16,256,694-16,256,714 CENPV
    nsv5547077insertion1nstd206human GRCh38 chr17: 16,345,411-16,345,411 , GRCh37.p13 chr17: 16,248,725-16,248,725 CENPV, PIGL
    nsv5517935copy number variation1nstd206human GRCh38 chr17: 16,345,275-16,345,411 , GRCh37.p13 chr17: 16,248,589-16,248,725 CENPV, PIGL
    nsv5150225mobile element insertion1nstd203human GRCh38 chr17: 16,345,411-16,345,424 , GRCh37.p13 chr17: 16,248,725-16,248,738 CENPV, PIGL
    nsv5148467mobile element insertion1nstd203human GRCh38 chr17: 16,345,409-16,345,424 , GRCh37.p13 chr17: 16,248,723-16,248,738 PIGL, CENPV
    nsv5140894mobile element insertion1nstd203human GRCh38 chr17: 16,345,414-16,345,424 , GRCh37.p13 chr17: 16,248,728-16,248,738 PIGL, CENPV
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729936copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,688,146-16,756,345 , GRCh38.p12 chr17: 15,784,832-16,853,031 ZNF624, RNU6-862P, 45 more genes
    nsv4729930copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,688,146-16,769,801 , GRCh38.p12 chr17: 15,784,832-16,866,487 LOC105371557, SPECC1P1, 45 more genes
    nsv4729738copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,810,015-18,537,436 , GRCh38.p12 chr17: 15,906,701-18,634,123 UPF3AP1, ADORA2B, 109 more genes
    nsv4721244insertion1nstd186human GRCh37 chr17: 16,248,738-16,248,738 , GRCh38.p12 chr17: 16,345,424-16,345,424 PIGL, CENPV
    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