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Items: 1 to 20 of 536

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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
    nsv7074639inversion1nstd229human GRCh38 chr18: 6,518,120-6,518,497 , GRCh37.p13 chr18: 6,518,119-6,518,496 LINC01387
    nsv7070666inversion1nstd229human GRCh38 chr18: 6,394,803-7,542,239 , GRCh37.p13 chr18: 6,394,802-7,542,237 ARHGAP28, LOC107985176, 19 more genes
    nsv7067886inversion1nstd229human GRCh38 chr18: 6,589,416-6,589,467 , GRCh37.p13 chr18: 6,589,415-6,589,466 LOC107985176, LINC01387
    nsv7067788inversion1nstd229human GRCh38 chr18: 6,518,070-6,523,206 , GRCh37.p13 chr18: 6,518,069-6,523,205 LINC01387
    nsv7066480inversion1nstd229human GRCh38 chr18: 6,514,173-6,518,461 , GRCh37.p13 chr18: 6,514,172-6,518,460 LINC01387
    nsv7064828inversion1nstd229human GRCh38 chr18: 6,351,167-7,375,513 , GRCh37.p13 chr18: 6,351,166-7,375,511 LOC107985176, RNU6-349P, 18 more genes
    nsv7061499inversion1nstd229human GRCh38 chr18: 6,455,100-6,548,637 , GRCh37.p13 chr18: 6,455,099-6,548,636 RPL6P27, LINC01387, 1 more genes
    nsv7017794copy number variation1nstd229human GRCh38 chr18: 6,569,364-6,569,438 , GRCh37.p13 chr18: 6,569,363-6,569,437 LINC01387, LOC107985176, 1 more genes
    nsv7017400copy number variation1nstd229human GRCh38 chr18: 6,534,389-6,537,568 , GRCh37.p13 chr18: 6,534,388-6,537,567 LINC01387
    nsv7016644copy number variation1nstd229human GRCh38 chr18: 6,547,162-6,883,864 , GRCh37.p13 chr18: 6,547,161-6,883,863 ARHGAP28, LOC105371972, 4 more genes
    nsv7016272copy number variation1nstd229human GRCh38 chr18: 6,307,737-7,184,933 , GRCh37.p13 chr18: 6,307,736-7,184,931 RPL6P27, LINC01387, 14 more genes
    nsv7015720copy number variation1nstd229human GRCh38 chr18: 6,438,207-6,523,649 , GRCh37.p13 chr18: 6,438,206-6,523,648 RNU6-349P, RPL6P27, 1 more genes
    nsv7015311copy number variation1nstd229human GRCh38 chr18: 6,514,801-6,520,100 , GRCh37.p13 chr18: 6,514,800-6,520,099 LINC01387
    nsv7015128copy number variation1nstd229human GRCh38 chr18: 4,434,377-14,413,632 , GRCh37.p13 chr18: 4,434,377-14,413,631 RAB31, THEMIS3P, 167 more genes
    nsv7011307copy number variation1nstd229human GRCh38 chr18: 6,584,796-6,589,590 , GRCh37.p13 chr18: 6,584,795-6,589,589 LOC107985176, LINC01387
    nsv7010384copy number variation1nstd229human GRCh38 chr18: 6,459,519-6,874,410 , GRCh37.p13 chr18: 6,459,518-6,874,409 LINC01387, LOC107985176, 5 more genes
    nsv7009965copy number variation1nstd229human GRCh38 chr18: 6,544,289-6,544,401 , GRCh37.p13 chr18: 6,544,288-6,544,400 LINC01387
    nsv7009907copy number variation1nstd229human GRCh38 chr18: 6,504,596-6,575,494 , GRCh37.p13 chr18: 6,504,595-6,575,493 LINC01387, LOC107985176, 1 more genes
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