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Items: 1 to 20 of 759

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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
    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
    nsv7010333copy number variation1nstd229human GRCh38 chr18: 14,768,987-14,784,468 , GRCh37.p13 chr18: 14,768,986-14,784,467 ANKRD30B, LOC105372008
    nsv7007961copy number variation1nstd229human GRCh38 chr18: 14,746,692-14,758,961 , GRCh37.p13 chr18: 14,746,691-14,758,960 RNU6-1210P, LOC105372007, 2 more genes
    nsv7007772copy number variation1nstd229human GRCh38 chr18: 13,577,365-14,771,703 , GRCh37.p13 chr18: 13,577,364-14,771,702 GRAMD4P7, RNU6-316P, 39 more genes
    nsv7007621copy number variation1nstd229human GRCh38 chr18: 14,755,620-14,773,383 , GRCh37.p13 chr18: 14,755,619-14,773,382 ANKRD30B, LOC105372008, 1 more genes
    nsv7005866copy number variation1nstd229human GRCh38 chr18: 14,741,547-14,763,336 , GRCh37.p13 chr18: 14,741,546-14,763,335 LOC105372008, ANKRD30B, 2 more genes
    nsv7005030copy number variation1nstd229human GRCh38 chr18: 14,791,111-14,807,855 , GRCh37.p13 chr18: 14,791,110-14,807,854 ANKRD30B
    nsv7004918copy number variation1nstd229human GRCh38 chr18: 14,793,355-14,795,820 , GRCh37.p13 chr18: 14,793,354-14,795,819 ANKRD30B
    nsv7002608copy number variation1nstd229human GRCh38 chr18: 14,770,201-14,772,500 , GRCh37.p13 chr18: 14,770,200-14,772,499 ANKRD30B
    nsv7000059copy number variation1nstd229human GRCh38 chr18: 14,798,836-14,799,342 , GRCh37.p13 chr18: 14,798,835-14,799,341 ANKRD30B
    nsv6999588copy number variation1nstd229human GRCh38 chr18: 14,752,509-14,752,669 , GRCh37.p13 chr18: 14,752,508-14,752,668 ANKRD30B
    nsv6998621copy number variation1nstd229human GRCh38 chr18: 14,821,938-14,825,913 , GRCh37.p13 chr18: 14,821,937-14,825,912 ANKRD30B
    nsv6998410copy number variation1nstd229human GRCh38 chr18: 14,747,614-14,747,982 , GRCh37.p13 chr18: 14,747,613-14,747,981 LOC105372007, ANKRD30B
    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
    nsv6624542copy number variation1nstd224human GRCh37 chr18: 14,660,464-14,791,236 , GRCh38.p12 chr18: 14,660,465-14,791,237 ANKRD30B, VN1R74P, 6 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
    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
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