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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076342inversion1nstd229human GRCh38 chr18: 36,552,732-40,928,121 , GRCh37.p13 chr18: 34,132,695-38,508,085 CELF4, LOC105372074, 32 more genes
    nsv7017830copy number variation1nstd229human GRCh38 chr18: 36,828,401-36,943,500 , GRCh37.p13 chr18: 34,408,364-34,523,463 LOC105372069, TPGS2, 1 more genes
    nsv7015372copy number variation1nstd229human GRCh38 chr18: 36,911,589-36,911,671 , GRCh37.p13 chr18: 34,491,552-34,491,634 KIAA1328, LOC105372069
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv7007198copy number variation1nstd229human GRCh38 chr18: 36,899,656-36,901,618 , GRCh37.p13 chr18: 34,479,619-34,481,581 LOC105372069, KIAA1328
    nsv7004194copy number variation1nstd229human GRCh38 chr18: 36,828,499-37,069,418 , GRCh37.p13 chr18: 34,408,462-34,649,381 KIAA1328, TPGS2, 1 more genes
    nsv6999227copy number variation1nstd229human GRCh38 chr18: 36,697,411-37,375,335 , GRCh37.p13 chr18: 34,277,374-34,955,298 FHOD3, KIAA1328, 4 more genes
    nsv6999143copy number variation1nstd229human GRCh38 chr18: 36,889,001-37,087,300 , GRCh37.p13 chr18: 34,468,964-34,667,263 LOC105372069, KIAA1328
    nsv6637962copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,908,661-35,007,766 , GRCh38.p12 chr18: 36,328,698-37,427,803 LOC105372071, TPGS2, 5 more genes
    nsv6637900copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,748,335-34,810,178 , GRCh38.p12 chr18: 36,168,372-37,230,215 FHOD3, MOCOS, 8 more genes
    nsv6637530copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,748,335-34,813,244 , GRCh38.p12 chr18: 36,168,372-37,233,281 MOCOS, KIAA1328, 8 more genes
    nsv6637267copy number variation1nstd102humanUncertain significance GRCh37 chr18: 34,278,224-34,957,600 , GRCh38.p12 chr18: 36,698,261-37,377,637 LOC105372069, FHOD3, 4 more genes
    nsv6624383copy number variation1nstd224human GRCh37 chr18: 33,918,700-34,675,985 , GRCh38.p12 chr18: 36,338,737-37,096,022 LOC105372071, KIAA1328, 3 more genes
    nsv6534602copy number variation1nstd223human GRCh38 chr18: 36,909,142-36,910,730 , GRCh37.p13 chr18: 34,489,105-34,490,693 LOC105372069, KIAA1328
    nsv6531753copy number variation1nstd223human GRCh38 chr18: 36,697,411-37,375,336 , GRCh37.p13 chr18: 34,277,374-34,955,299 LOC105372068, TPGS2, 4 more genes
    nsv6528596copy number variation1nstd223human GRCh38 chr18: 36,918,658-36,990,690 , GRCh37.p13 chr18: 34,498,621-34,570,653 KIAA1328, LOC105372069
    nsv6522892copy number variation1nstd223human GRCh38 chr18: 36,912,104-36,912,631 , GRCh37.p13 chr18: 34,492,067-34,492,594 LOC105372069, KIAA1328
    nsv6518026copy number variation1nstd223human GRCh38 chr18: 36,828,409-36,943,546 , GRCh37.p13 chr18: 34,408,372-34,523,509 KIAA1328, TPGS2, 1 more genes
    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
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