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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7099268copy number variation1nstd231human GRCh38.p12 chr1: 236,219,923-236,467,563 , GRCh37 chr1: 236,383,223-236,630,863 ERO1B, EDARADD, 2 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv7040505inversion1nstd229human GRCh38 chr1: 235,226,873-236,268,697 , GRCh37.p13 chr1: 235,390,188-236,431,997 RPS21P1, NID1, 26 more genes
    nsv6677584copy number variation1nstd229human GRCh38 chr1: 236,211,825-236,216,028 , GRCh37.p13 chr1: 236,375,125-236,379,328 ERO1B, GPR137B
    nsv6673582copy number variation1nstd229human GRCh38 chr1: 236,198,601-236,235,600 , GRCh37.p13 chr1: 236,361,901-236,398,900 GPR137B, ERO1B
    nsv6669357copy number variation1nstd229human GRCh38 chr1: 236,250,587-236,250,620 , GRCh37.p13 chr1: 236,413,887-236,413,920 ERO1B
    nsv6669086copy number variation1nstd229human GRCh38 chr1: 236,178,821-236,566,887 , GRCh37.p13 chr1: 236,342,121-236,730,187 LGALS8, LGALS8-AS1, 7 more genes
    nsv6668135copy number variation1nstd229human GRCh38 chr1: 236,228,294-236,265,947 , GRCh37.p13 chr1: 236,391,594-236,429,247 RNU2-70P, ERO1B
    nsv6667646copy number variation1nstd229human GRCh38 chr1: 236,267,333-236,267,458 , GRCh37.p13 chr1: 236,430,633-236,430,758 RNU2-70P, ERO1B
    nsv6666087copy number variation1nstd229human GRCh38 chr1: 236,212,101-236,416,200 , GRCh37.p13 chr1: 236,375,401-236,579,500 RNU2-70P, GPR137B, 3 more genes
    nsv6662257copy number variation1nstd229human GRCh38 chr1: 236,253,901-236,547,900 , GRCh37.p13 chr1: 236,417,201-236,711,200 HEATR1, LOC100130485, 6 more genes
    nsv6661754copy number variation1nstd229human GRCh38 chr1: 236,182,764-236,747,255 , GRCh37.p13 chr1: 236,346,064-236,910,555 HEATR1, RNU2-70P, 8 more genes
    nsv6659835copy number variation1nstd229human GRCh38 chr1: 236,269,396-236,269,435 , GRCh37.p13 chr1: 236,432,696-236,432,735 ERO1B
    nsv6659688copy number variation1nstd229human GRCh38 chr1: 235,760,337-236,349,480 , GRCh37.p13 chr1: 235,923,637-236,512,780 LOC100130485, RNU6-968P, 10 more genes
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
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