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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5071410mobile element insertion1nstd203human GRCh38 chr1: 171,325,865-171,325,865 , GRCh37.p13 chr1: 171,295,004-171,295,004 FMO4
    nsv5067118mobile element insertion1nstd203human GRCh38 chr1: 171,325,817-171,325,865 , GRCh37.p13 chr1: 171,294,956-171,295,004 FMO4
    nsv4898022copy number variation1nstd200human GRCh38 chr1: 171,325,089-171,410,428 , GRCh37.p13 chr1: 171,294,228-171,379,567 GM2AP2, SRP14P4, 2 more genes
    nsv4784664copy number variation1nstd200human GRCh37 chr1: 171,294,228-171,379,567 , GRCh38.p12 chr1: 171,325,089-171,410,428 GM2AP2, TOP1P1, 2 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
    nsv4674768copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480 ATP1B1, RNU6-693P, 156 more genes
    nsv4674474copy number variation1nstd102humanUncertain significance GRCh37 chr1: 171,048,831-171,338,651 , GRCh38.p12 chr1: 171,079,690-171,369,512 FMO4, FMO6P, 10 more genes
    nsv4594078copy number variation1nstd183human GRCh37 chr1: 171,128,845-171,414,611 , GRCh38.p12 chr1: 171,159,706-171,445,472 FMO1, CYCSP53, 9 more genes
    nsv4594077copy number variation1nstd183human GRCh37 chr1: 171,016,086-171,726,961 , GRCh38.p12 chr1: 171,046,945-171,757,821 MYOCOS, PFN1P1, 23 more genes
    nsv4569425sequence alteration1nstd166human GRCh37.p13 chr1: 171,302,980-171,302,981 , GRCh38.p12 chr1: 171,333,841-171,333,842 FMO4
    nsv4451273copy number variation1nstd102humanUncertain significance GRCh37 chr1: 170,862,952-171,480,090 , GRCh38.p12 chr1: 170,893,811-171,510,951 CYCSP53, PRRC2C, 16 more genes
    nsv4346686copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,423,492-180,367,623 , GRCh38.p12 chr1: 169,454,254-180,398,488 TNFSF4, MIR3119-1, 202 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 LINC00626, RN7SL861P, 359 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4068070copy number variation1nstd166human GRCh37.p13 chr1: 171,280,923-171,281,391 , GRCh38.p12 chr1: 171,311,784-171,312,252 FMO4
    nsv4065028copy number variation1nstd166human GRCh37.p13 chr1: 171,289,938-171,289,996 , GRCh38.p12 chr1: 171,320,799-171,320,857 FMO4
    nsv4058931copy number variation1nstd166human GRCh37.p13 chr1: 171,294,228-171,379,567 , GRCh38.p12 chr1: 171,325,089-171,410,428 GM2AP2, FMO4, 2 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
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