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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5828344copy number variation1nstd209human GRCh37.p13 chr1|NW_003871055.3: 6,653,503-6,665,656 , GRCh38 chr1: 149,838,090-149,850,243 , GRCh37.p13 chr1: 149,809,652-149,821,810 H2BC20P, H2BC19P, 3 more genes
    nsv5672211inversion1nstd207human GRCh38 chr1: 149,817,539-149,876,316 , GRCh37.p13 chr1: 149,789,093-149,847,866 , GRCh37.p13 chr1|NW_003871055.3: 6,632,952-6,691,729 H2AC18, H4C14, 6 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4730064inversion26nstd198human GRCh38 chr1: 149,816,748-149,876,338 , GRCh37.p13 chr1: 149,788,302-149,847,888 , GRCh37.p13 chr1|NW_003871055.3: 6,632,161-6,691,751 H2AC18, H4C14, 6 more genes
    nsv4579553copy number variation1nstd183human GRCh37 chr1: 149,791,739-149,872,081 , GRCh38.p12 chr1: 149,820,184-149,900,528 H2BC21, H4C15, 10 more genes
    nsv4579291copy number variation1nstd183human GRCh37 chr1: 149,788,216-149,857,110 , GRCh38.p12 chr1: 149,816,662-149,885,560 H3C15, H2AC19, 9 more genes
    nsv4386636copy number variation1nstd173human GRCh37 chr1: 149,803,428-149,825,762 , GRCh38.p12 chr1: 149,831,864-149,854,200 H2AC18, H4C14, 5 more genes
    nsv4071431copy number variation1nstd166human GRCh37.p13 chr1: 149,806,000-149,815,500 , GRCh38.p12 chr1: 149,834,434-149,843,933 H2BC19P, H2AC18, 1 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
    nsv3885263copy number variation1nstd102humanBenign GRCh37 chr1: 149,789,016-149,835,093 , GRCh38.p12 chr1: 149,817,462-149,863,527 H2AC18, H4C14, 6 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 more genes
    nsv3884446copy number variation1nstd102humanUncertain significance GRCh37 chr1: 149,802,401-149,944,241 , GRCh38.p12 chr1: 149,830,837-149,972,313 H3C14, H2AC21, 14 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 , RNU1-153P, 4887 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , MARK1, 4930 more genes
    nsv3247411inversion9nstd152human GRCh38 chr1: 149,820,002-149,876,339 , GRCh37.p13 chr1: 149,791,557-149,847,889 , GRCh37.p13 chr1|NW_003871055.3: 6,635,415-6,691,752 H2AC18, H4C14, 6 more genes
    nsv3228503insertion1nstd152human GRCh38 chr1: 149,836,081-149,839,851 , GRCh37.p13 chr1: 149,807,643-149,811,423 , GRCh37.p13 chr1|NW_003871055.3: 6,651,494-6,655,264 H3C14
    nsv3168056copy number variation1nstd158human GRCh38.p12 chr1: 84,243,714-179,997,709 , GRCh37 chr1: 84,709,397-179,966,844 , ABCA4, 1909 more genes
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