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Items: 1 to 20 of 279

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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
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    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
    nsv7012063copy number variation1nstd229human GRCh38 chr18: 12,719,130-12,784,114 , GRCh37.p13 chr18: 12,719,129-12,784,113 LINC01882, PSMG2, 1 more genes
    nsv7010603copy number variation1nstd229human GRCh38 chr18: 12,597,906-12,834,055 , GRCh37.p13 chr18: 12,597,905-12,834,054 LINC01882, CEP76, 3 more genes
    nsv7010168copy number variation1nstd229human GRCh38 chr18: 12,747,447-12,754,888 , GRCh37.p13 chr18: 12,747,446-12,754,887 LINC01882
    nsv7009756copy number variation1nstd229human GRCh38 chr18: 12,483,561-12,800,777 , GRCh37.p13 chr18: 12,483,560-12,800,776 CEP76, PTPN2, 3 more genes
    nsv7009670copy number variation1nstd229human GRCh38 chr18: 12,744,580-12,747,703 , GRCh37.p13 chr18: 12,744,579-12,747,702 LINC01882
    nsv7005396copy number variation1nstd229human GRCh38 chr18: 12,744,403-12,753,802 , GRCh37.p13 chr18: 12,744,402-12,753,801 LINC01882
    nsv7004677copy number variation1nstd229human GRCh38 chr18: 12,744,238-12,753,120 , GRCh37.p13 chr18: 12,744,237-12,753,119 LINC01882
    nsv7003207copy number variation1nstd229human GRCh38 chr18: 11,244,551-12,953,481 , GRCh37.p13 chr18: 11,244,550-12,953,480 LINC01255, AFG3L2, 41 more genes
    nsv7002363copy number variation1nstd229human GRCh38 chr18: 12,747,691-12,748,666 , GRCh37.p13 chr18: 12,747,690-12,748,665 LINC01882
    nsv6999801copy number variation1nstd229human GRCh38 chr18: 12,000,674-12,871,099 , GRCh37.p13 chr18: 12,000,673-12,871,098 RNU6-170P, ANKRD62, 24 more genes
    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
    nsv6624539copy number variation1nstd224human GRCh37 chr18: 12,686,398-12,779,947 , GRCh38.p12 chr18: 12,686,399-12,779,948 CEP76, PSMG2, 1 more genes
    nsv6534697copy number variation1nstd223human GRCh38 chr18: 12,719,130-12,784,116 , GRCh37.p13 chr18: 12,719,129-12,784,115 LINC01882, PSMG2, 1 more genes
    nsv6532714copy number variation1nstd223human GRCh38 chr18: 12,746,812-12,747,757 , GRCh37.p13 chr18: 12,746,811-12,747,756 LINC01882
    nsv6524805copy number variation1nstd223human GRCh38 chr18: 12,742,505-12,744,925 , GRCh37.p13 chr18: 12,742,504-12,744,924 LINC01882
    nsv6524552copy number variation1nstd223human GRCh38 chr18: 12,045,864-12,921,903 , GRCh37.p13 chr18: 12,045,863-12,921,902 RNU6-170P, ANKRD62, 25 more genes
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