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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885112copy number variation1nstd209human GRCh38 chr1: 156,344,707-156,346,765 , GRCh37.p13 chr1: 156,314,498-156,316,556 TSACC
    nsv5876693copy number variation1nstd209human GRCh38 chr1: 156,339,789-156,344,576 , GRCh37.p13 chr1: 156,309,580-156,314,367 TSACC
    nsv5623919insertion1nstd207human GRCh38 chr1: 156,344,739-156,344,739 , GRCh37.p13 chr1: 156,314,530-156,314,530 TSACC
    nsv5559729sequence alteration1nstd206human GRCh38 chr1: 156,338,639-156,344,748 , GRCh37.p13 chr1: 156,308,430-156,314,539 CCT3, TSACC
    nsv5552857insertion1nstd206human GRCh38 chr1: 156,344,739-156,344,739 , GRCh37.p13 chr1: 156,314,530-156,314,530 TSACC
    nsv5423596copy number variation1nstd206human GRCh38 chr1: 156,342,400-156,343,341 , GRCh37.p13 chr1: 156,312,191-156,313,132 TSACC
    nsv5422820copy number variation1nstd206human GRCh38 chr1: 156,345,312-156,345,417 , GRCh37.p13 chr1: 156,315,103-156,315,208 TSACC
    nsv5421884copy number variation1nstd206human GRCh38 chr1: 156,321,025-156,354,439 , GRCh37.p13 chr1: 156,290,816-156,324,230 TSACC, CCT3
    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
    nsv5296489copy number variation1nstd204human GRCh37.p13 chr1: 156,306,480-156,306,591 , GRCh38.p13 chr1: 156,336,689-156,336,800 CCT3, TSACC
    nsv4784338copy number variation1nstd200human GRCh37 chr1: 156,310,241-156,310,506 , GRCh38.p12 chr1: 156,340,450-156,340,715 TSACC
    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
    nsv4579743copy number variation1nstd183human GRCh37 chr1: 156,308,124-156,308,697 , GRCh38.p12 chr1: 156,338,333-156,338,906 TSACC, CCT3
    nsv4579382copy number variation1nstd183human GRCh37 chr1: 156,307,182-156,309,347 , GRCh38.p12 chr1: 156,337,391-156,339,556 TSACC, CCT3
    nsv4535086insertion1nstd166human GRCh37.p13 chr1: 156,316,729-156,316,729 , GRCh38.p12 chr1: 156,346,938-156,346,938 TSACC
    nsv4452451copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,037,369-156,463,980 , GRCh38.p12 chr1: 156,067,578-156,494,188 MIR9-1HG, TSACC, 17 more genes
    nsv4452342copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,770,505-156,652,136 , GRCh38.p12 chr1: 155,800,714-156,682,344 NES, SNORA80E, 43 more genes
    nsv4389283copy number variation1nstd171human GRCh37 chr1: 156,306,102-156,306,138 , GRCh38.p12 chr1: 156,336,311-156,336,347 CCT3, TSACC
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
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