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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
    nsv7095258copy number variation1nstd102humanUncertain significance GRCh37 chr18: 9,102,742-12,725,530 , GRCh38.p12 chr18: 9,102,744-12,725,531 PIEZO2, RALBP1, 77 more genes
    nsv7076310inversion1nstd229human GRCh38 chr18: 7,168,687-9,983,107 , GRCh37.p13 chr18: 7,168,686-9,983,104 MTCL1, LOC112577592, 40 more genes
    nsv7074432inversion1nstd229human GRCh38 chr18: 9,566,178-9,566,301 , GRCh37.p13 chr18: 9,566,176-9,566,299 PPP4R1
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7072227inversion1nstd229human GRCh38 chr18: 9,565,943-9,571,287 , GRCh37.p13 chr18: 9,565,941-9,571,285 PPP4R1
    nsv7063546inversion1nstd229human GRCh38 chr18: 9,568,675-9,571,025 , GRCh37.p13 chr18: 9,568,673-9,571,023 PPP4R1
    nsv7017910copy number variation1nstd229human GRCh38 chr18: 9,596,751-9,599,105 , GRCh37.p13 chr18: 9,596,749-9,599,103 PPP4R1
    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
    nsv7011753copy number variation1nstd229human GRCh38 chr18: 9,469,501-9,562,000 , GRCh37.p13 chr18: 9,469,499-9,561,998 RNU2-27P, RALBP1, 2 more genes
    nsv7009620copy number variation1nstd229human GRCh38 chr18: 9,611,998-9,635,001 , GRCh37.p13 chr18: 9,611,996-9,634,999 PPP4R1, RNU6-903P, 1 more genes
    nsv7004750copy number variation1nstd229human GRCh38 chr18: 9,564,562-9,568,457 , GRCh37.p13 chr18: 9,564,560-9,568,455 PPP4R1
    nsv7002580copy number variation1nstd229human GRCh38 chr18: 9,607,001-9,786,800 , GRCh37.p13 chr18: 9,606,999-9,786,797 KRT18P8, LINC02856, 6 more genes
    nsv7000272copy number variation1nstd229human GRCh38 chr18: 9,584,828-9,588,088 , GRCh37.p13 chr18: 9,584,826-9,588,086 PPP4R1
    nsv6998883copy number variation1nstd229human GRCh38 chr18: 9,563,513-9,563,696 , GRCh37.p13 chr18: 9,563,511-9,563,694 PPP4R1
    nsv6637624copy number variation1nstd102humanUncertain significance GRCh37 chr18: 8,585,096-9,660,466 , GRCh38.p12 chr18: 8,585,098-9,660,468 TWSG1-DT, RPS4XP19, 16 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
    nsv6578158inversion1nstd223human GRCh38 chr18: 9,607,098-9,607,720 , GRCh37.p13 chr18: 9,607,096-9,607,718 PPP4R1
    nsv6576534inversion1nstd223human GRCh38 chr18: 9,566,014-9,566,543 , GRCh37.p13 chr18: 9,566,012-9,566,541 PPP4R1
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