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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682112copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 161,789,423-161,790,951 , GRCh38.p12 chr1: 161,819,633-161,821,161 ATF6
    nsv6310599copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 161,748,014-161,748,130 , GRCh38.p12 chr1: 161,778,224-161,778,340 ATF6
    nsv3880578copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,726,804-161,867,948 , GRCh38.p12 chr1: 161,757,014-161,898,158 ATF6, LOC100422526, 2 more genes
    nsv6310600copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,816,219-162,040,092 , GRCh38.p12 chr1: 161,846,429-162,070,302 ATF6, LOC100422526, 2 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 ATF6, CRB1, 1608 more genes
    nsv3873192copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589 ATF6, COLGALT2, 402 more genes
    nsv3889882copy number variation1nstd102humanPathogenic GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847 ATF6, FMO4, 403 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 ATF6, LINC00626, 359 more genes
    nsv3894431copy number variation1nstd102humanPathogenic NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154 ATF6, RPL21P27, 238 more genes
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 ATF6, FCGR3B, 302 more genes
    nsv3906717copy number variation1nstd102humanPathogenic GRCh38 chr1: 159,479,887-166,895,086 , GRCh37 chr1: 159,449,677-166,864,323 , NCBI36 chr1: 157,716,301-165,130,947 ATF6, NOS1AP, 220 more genes
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 ATF6, USF1, 161 more genes
    nsv3884593copy number variation1nstd102humanPathogenic NCBI36 chr1: 157,610,062-160,185,096 , GRCh37.p13 chr1: 159,343,438-161,918,472 , GRCh38.p12 chr1: 159,373,648-161,948,682 ATF6, OR10AE1P, 148 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 ATF6, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 ATF6, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 ATF6, RNU1-153P, 4887 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 ATF6, LOC101060227, 1608 more genes
    nsv3900459copy number variation1nstd102humanPathogenic GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332 ATF6, HORMAD1, 923 more genes
    nsv3890224copy number variation1nstd102humanPathogenic GRCh38 chr1: 157,747,246-176,021,247 , GRCh37 chr1: 157,717,036-175,990,383 , NCBI36 chr1: 155,983,660-174,257,006 ATF6, LOC101928596, 475 more genes
    nsv6637132copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 161,924,068-164,761,399 , GRCh38.p12 chr1: 161,954,278-164,792,162 ATF6, DDR2, 33 more genes
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