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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7073714inversion1nstd229human GRCh38 chr18: 3,532,528-3,661,721 , GRCh37.p13 chr18: 3,532,526-3,661,721 DLGAP1-AS1, DLGAP1, 4 more genes
    nsv7060186inversion1nstd229human GRCh38 chr18: 3,609,290-3,610,110 , GRCh37.p13 chr18: 3,609,288-3,610,108 DLGAP1-AS2, DLGAP1
    nsv7014486copy number variation1nstd229human GRCh38 chr18: 3,393,401-3,715,600 , GRCh37.p13 chr18: 3,393,399-3,715,600 LOC105371967, GAPLINC, 10 more genes
    nsv7011136copy number variation1nstd229human GRCh38 chr18: 3,539,501-3,603,000 , GRCh37.p13 chr18: 3,539,499-3,602,998 DLGAP1, DLGAP1-AS2, 3 more genes
    nsv7006120copy number variation1nstd229human GRCh38 chr18: 3,606,009-3,614,853 , GRCh37.p13 chr18: 3,606,007-3,614,852 DLGAP1-AS2, DLGAP1
    nsv6999202copy number variation1nstd229human GRCh38 chr18: 3,503,801-3,708,300 , GRCh37.p13 chr18: 3,503,799-3,708,300 RN7SL39P, LOC100419892, 4 more genes
    nsv6637665copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,255,007-4,488,934 , GRCh38.p12 chr18: 2,255,007-4,488,934 DLGAP1-AS4, MYL12-AS1, 38 more genes
    nsv6637580copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-7,218,594 , GRCh38.p12 chr18: 136,227-7,218,596 L3MBTL4-AS1, LOC101927044, 106 more genes
    nsv6637521copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,485,817-4,086,341 , GRCh38.p12 chr18: 2,485,818-4,086,341 DLGAP1-AS4, EMILIN2, 35 more genes
    nsv6637285copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-11,283,184 , GRCh38.p12 chr18: 136,227-11,283,185 EMILIN2, KRT18P8, 165 more genes
    nsv6634418copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-8,638,260 , GRCh38.p12 chr18: 10,001-8,638,262 AKAIN1, LPIN2, 126 more genes
    nsv6624589copy number variation1nstd224human GRCh37 chr18: 3,414,008-3,729,292 , GRCh38.p12 chr18: 3,414,010-3,729,292 LOC100419892, TGIF1, 8 more genes
    nsv6588138inversion1nstd223human GRCh38 chr18: 3,608,158-3,608,884 , GRCh37.p13 chr18: 3,608,156-3,608,882 DLGAP1-AS2, DLGAP1
    nsv6585584inversion1nstd223human GRCh38 chr18: 3,134,944-5,291,746 , GRCh37.p13 chr18: 3,134,942-5,291,745 LINC00667, LINC01895, 33 more genes
    nsv6584800inversion1nstd223human GRCh38 chr18: 3,608,266-3,609,001 , GRCh37.p13 chr18: 3,608,264-3,608,999 DLGAP1-AS2, DLGAP1
    nsv6315536copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-10,172,941 , GRCh38.p12 chr18: 136,226-10,172,944 DLGAP1-AS5, TWSG1, 150 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315508copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-14,632,436 , GRCh38.p12 chr18: 136,226-14,632,437 IGLJCOR18, MYOM1, 247 more genes
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