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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7015345copy number variation1nstd229human GRCh38 chr18: 14,965,764-14,972,043 , GRCh37.p13 chr18: 14,965,763-14,972,042 LINC01443, LINC01444
    nsv7011056copy number variation1nstd229human GRCh38 chr18: 14,071,852-14,980,918 , GRCh37.p13 chr18: 14,071,851-14,980,917 OR4K7P, POTEC, 36 more genes
    nsv7007531copy number variation1nstd229human GRCh38 chr18: 14,959,193-14,968,634 , GRCh37.p13 chr18: 14,959,192-14,968,633 LINC01443, LINC01444
    nsv7005263copy number variation1nstd229human GRCh38 chr18: 14,968,985-14,977,078 , GRCh37.p13 chr18: 14,968,984-14,977,077 LINC01444, LINC01443
    nsv7003866copy number variation1nstd229human GRCh38 chr18: 14,954,637-14,978,828 , GRCh37.p13 chr18: 14,954,636-14,978,827 LINC01443, LINC01444
    nsv6637316copy number variation1nstd102humanUncertain significance GRCh37 chr18: 11,290,617-15,106,305 , GRCh38.p12 chr18: 11,290,618-15,106,306 SNX19P3, LDLRAD4, 96 more genes
    nsv6624331copy number variation1nstd224human GRCh37 chr18: 14,715,283-15,286,251 , GRCh38.p12 chr18: 14,715,284-15,286,252 LOC284269, LINC01443, 16 more genes
    nsv6624137copy number variation1nstd224human GRCh37 chr18: 14,912,796-15,286,251 , GRCh38.p12 chr18: 14,912,797-15,286,252 LINC01444, LINC01906, 8 more genes
    nsv6624136copy number variation1nstd224human GRCh37 chr18: 14,771,484-15,286,251 , GRCh38.p12 chr18: 14,771,485-15,286,252 FGF7P1, ANKRD30B, 11 more genes
    nsv6624135copy number variation4nstd224human GRCh37 chr18: 14,727,931-15,102,421 , GRCh38.p12 chr18: 14,727,932-15,102,422 ANKRD30B, MIR3156-2, 11 more genes
    nsv6533957copy number variation1nstd223human GRCh38 chr18: 14,965,764-14,972,040 , GRCh37.p13 chr18: 14,965,763-14,972,039 LINC01444, LINC01443
    nsv6525287copy number variation1nstd223human GRCh38 chr18: 14,968,984-14,977,077 , GRCh37.p13 chr18: 14,968,983-14,977,076 LINC01444, LINC01443
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6314195copy number variation1nstd102humanUncertain significance GRCh37 chr18: 14,715,282-18,988,457 , GRCh38.p12 chr18: 14,715,283-21,408,496 LOC105372008, LOC284269, 26 more genes
    nsv6291808copy number variation1nstd102humanLikely benign GRCh37 chr18: 14,710,374-15,181,666 , GRCh38.p12 chr18: 14,710,375-15,181,667 LINC01444, LOC105372010, 12 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
    nsv6290328copy number variation1nstd102humanPathogenic GRCh37 chr18: 10,501-15,410,398 , GRCh38.p12 chr18: 10,501-15,410,399 RNA5SP449, MPPE1, 275 more genes
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