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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
    nsv7141563insertion1nstd232human GRCh37.p13 chr18: 3,272,249-3,272,249 , GRCh38.p12 chr18: 3,272,251-3,272,251 MYL12B
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7094930copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,656,075-3,457,938 , GRCh38.p12 chr18: 2,656,076-3,457,940 EMILIN2, RNU7-25P, 16 more genes
    nsv7015933copy number variation1nstd229human GRCh38 chr18: 3,274,701-3,284,600 , GRCh37.p13 chr18: 3,274,699-3,284,598 MYL12B
    nsv7014963copy number variation1nstd229human GRCh38 chr18: 3,274,753-3,284,551 , GRCh37.p13 chr18: 3,274,751-3,284,549 MYL12B
    nsv7012077copy number variation1nstd229human GRCh38 chr18: 3,273,083-3,277,250 , GRCh37.p13 chr18: 3,273,081-3,277,248 MYL12B
    nsv7008356copy number variation1nstd229human GRCh38 chr18: 2,884,913-3,403,663 , GRCh37.p13 chr18: 2,884,911-3,403,661 SNRPCP4, LINC01895, 12 more genes
    nsv7007010copy number variation1nstd229human GRCh38 chr18: 3,269,711-3,269,786 , GRCh37.p13 chr18: 3,269,709-3,269,784 MYL12B
    nsv7000349copy number variation1nstd229human GRCh38 chr18: 3,196,901-3,290,400 , GRCh37.p13 chr18: 3,196,899-3,290,398 LOC101927044, MYL12B, 3 more genes
    nsv6637684copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,818,532-3,412,231 , GRCh38.p12 chr18: 2,818,534-3,412,233 RPL31P59, IGLJCOR18, 14 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
    nsv6637535copy number variation1nstd102humanUncertain significance GRCh37 chr18: 3,031,067-3,363,755 , GRCh38.p12 chr18: 3,031,069-3,363,757 LOC101927044, MYL12B, 5 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
    nsv6624587copy number variation1nstd224human GRCh37 chr18: 3,046,986-3,287,105 , GRCh38.p12 chr18: 3,046,988-3,287,107 MYOM1, MYL12A, 4 more genes
    nsv6624583copy number variation1nstd224human GRCh37 chr18: 2,881,839-3,319,915 , GRCh38.p12 chr18: 2,881,841-3,319,917 MYOM1, EMILIN2, 9 more genes
    nsv6624148copy number variation1nstd224human GRCh37 chr18: 2,920,311-3,401,411 , GRCh38.p12 chr18: 2,920,313-3,401,413 LPIN2, MYL12A, 11 more genes
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