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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
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7069734inversion1nstd229human GRCh38 chr18: 12,681,735-12,689,451 , GRCh37.p13 chr18: 12,681,734-12,689,450 PSMG2, CEP76
    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
    nsv7011791copy number variation1nstd229human GRCh38 chr18: 12,709,789-12,716,684 , GRCh37.p13 chr18: 12,709,788-12,716,683 PSMG2
    nsv7011439copy number variation1nstd229human GRCh38 chr18: 12,630,301-12,685,900 , GRCh37.p13 chr18: 12,630,300-12,685,899 CEP76, PSMG2, 1 more genes
    nsv7011004copy number variation1nstd229human GRCh38 chr18: 12,714,525-12,720,107 , GRCh37.p13 chr18: 12,714,524-12,720,106 PSMG2
    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
    nsv7010527copy number variation1nstd229human GRCh38 chr18: 12,689,672-12,690,565 , GRCh37.p13 chr18: 12,689,671-12,690,564 CEP76, PSMG2
    nsv7010186copy number variation1nstd229human GRCh38 chr18: 12,710,981-12,727,617 , GRCh37.p13 chr18: 12,710,980-12,727,616 PSMG2
    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
    nsv7006630copy number variation1nstd229human GRCh38 chr18: 12,702,436-12,725,764 , GRCh37.p13 chr18: 12,702,435-12,725,763 PSMG2, CEP76
    nsv7005896copy number variation1nstd229human GRCh38 chr18: 12,698,004-12,699,000 , GRCh37.p13 chr18: 12,698,003-12,698,999 PSMG2, CEP76
    nsv7005271copy number variation1nstd229human GRCh38 chr18: 12,657,223-12,657,273 , GRCh37.p13 chr18: 12,657,222-12,657,272 PSMG2, SPIRE1
    nsv7004378copy number variation1nstd229human GRCh38 chr18: 12,617,141-12,691,708 , GRCh37.p13 chr18: 12,617,140-12,691,707 CEP76, SPIRE1, 1 more genes
    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
    nsv7000065copy number variation1nstd229human GRCh38 chr18: 12,637,101-12,668,000 , GRCh37.p13 chr18: 12,637,100-12,667,999 PSMG2, SPIRE1, 1 more genes
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