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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950819insertion1nstd209human GRCh38 chr1: 224,407,143-224,407,143 , GRCh37.p13 chr1: 224,594,845-224,594,845 WDR26
    nsv5884342copy number variation1nstd209human GRCh38 chr1: 221,964,560-227,275,238 , GRCh37.p13 chr1: 222,137,902-227,462,939 , YBX1P9, 111 more genes
    nsv5444670copy number variation1nstd206human GRCh38 chr1: 224,430,105-224,430,277 , GRCh37.p13 chr1: 224,617,807-224,617,979 WDR26
    nsv5407944mobile element insertion1nstd206human GRCh38 chr1: 224,406,804-224,406,855 , GRCh37.p13 chr1: 224,594,506-224,594,557 WDR26
    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
    nsv5201042copy number variation1nstd204human GRCh38.p13 chr1: 224,399,807-224,402,258 , GRCh37.p13 chr1: 224,587,509-224,589,960 WDR26
    nsv5200338copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,552,998-224,761,890 , GRCh38.p12 chr1: 223,379,656-224,574,188 LOC105373025, CAPN2, 32 more genes
    nsv5073779mobile element insertion1nstd203human GRCh38 chr1: 224,406,788-224,406,804 , GRCh37.p13 chr1: 224,594,490-224,594,506 WDR26
    nsv5069310mobile element insertion1nstd203human GRCh38 chr1: 224,406,305-224,406,320 , GRCh37.p13 chr1: 224,594,007-224,594,022 WDR26
    nsv5066737mobile element insertion1nstd203human GRCh38 chr1: 224,407,122-224,407,168 , GRCh37.p13 chr1: 224,594,824-224,594,870 WDR26
    nsv5064243mobile element insertion1nstd203human GRCh38 chr1: 224,406,787-224,406,803 , GRCh37.p13 chr1: 224,594,489-224,594,505 WDR26
    nsv4898964copy number variation1nstd200human GRCh38 chr1: 224,407,075-224,410,268 , GRCh37.p13 chr1: 224,594,777-224,597,970 WDR26
    nsv4898963copy number variation1nstd200human GRCh38 chr1: 224,402,452-224,402,575 , GRCh37.p13 chr1: 224,590,154-224,590,277 WDR26
    nsv4898957copy number variation1nstd200human GRCh38 chr1: 224,242,609-224,951,746 , GRCh37.p13 chr1: 224,430,311-225,139,448 LINC02813, NVL, 13 more genes
    nsv4774573copy number variation1nstd200human GRCh37 chr1: 224,594,777-224,597,970 , GRCh38.p12 chr1: 224,407,075-224,410,268 WDR26
    nsv4774572copy number variation1nstd200human GRCh37 chr1: 224,590,154-224,590,277 , GRCh38.p12 chr1: 224,402,452-224,402,575 WDR26
    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
    nsv4728731copy number variation1nstd102humanPathogenic GRCh37 chr1: 224,442,473-224,794,913 , GRCh38.p12 chr1: 224,254,771-224,607,211 NVL, CNIH4, 7 more genes
    nsv4728176copy number variation1nstd102humanPathogenic GRCh37 chr1: 222,605,125-224,696,628 , GRCh38.p12 chr1: 222,431,783-224,508,926 SEPTIN7P13, LOC101927164, 52 more genes
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