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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7094312copy number variation2nstd102humanUncertain significance GRCh37 chr15: 89,379,429-91,565,479 , GRCh38.p12 chr15: 88,836,198-91,022,249 IQGAP1, WDR93, 77 more genes
    nsv7068128inversion1nstd229human GRCh38 chr15: 87,287,023-90,484,635 , GRCh37.p13 chr15: 87,830,254-91,027,867 , LOC105370964, 81 more genes
    nsv7065612inversion1nstd229human GRCh38 chr15: 89,041,442-91,616,740 , GRCh37.p13 chr15: 89,584,673-92,159,970 ZNF774, CRAT37, 77 more genes
    nsv7062993inversion1nstd229human GRCh38 chr15: 85,570,479-90,463,746 , GRCh37.p13 chr15: 86,113,710-91,006,978 , NTRK3-AS1, 97 more genes
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6968835copy number variation1nstd229human GRCh38 chr15: 89,675,751-89,684,378 , GRCh37.p13 chr15: 90,218,982-90,227,609 PLIN1, PEX11A
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6635762copy number variation1nstd227human GRCh38.p12 chr15: 89,673,865-89,692,979 , GRCh37 chr15: 90,217,096-90,236,210 PLIN1, PEX11A, 2 more genes
    nsv6623353copy number variation1nstd224human GRCh37 chr15: 90,100,100-90,275,206 , GRCh38.p12 chr15: 89,556,869-89,731,975 PLIN1, PEX11A, 5 more genes
    nsv6623291copy number variation1nstd224human GRCh37 chr15: 90,226,642-90,255,555 , GRCh38.p12 chr15: 89,683,411-89,712,324 WDR93, RPL36AP43, 2 more genes
    nsv6623290copy number variation1nstd224human GRCh37 chr15: 90,226,642-90,245,281 , GRCh38.p12 chr15: 89,683,411-89,702,050 PEX11A, WDR93, 1 more genes
    nsv6582041inversion1nstd223human GRCh38 chr15: 85,570,476-90,463,749 , GRCh37.p13 chr15: 86,113,707-91,006,981 , AP3S2, 97 more genes
    nsv6503799copy number variation1nstd223human GRCh38 chr15: 89,676,601-89,737,100 , GRCh37.p13 chr15: 90,219,832-90,280,331 PLIN1, PEX11A, 4 more genes
    nsv6500255copy number variation1nstd223human GRCh38 chr15: 89,688,926-89,697,991 , GRCh37.p13 chr15: 90,232,157-90,241,222 PEX11A, WDR93
    nsv6497938copy number variation1nstd223human GRCh38 chr15: 89,676,529-89,694,507 , GRCh37.p13 chr15: 90,219,760-90,237,738 RPL36AP43, WDR93, 2 more genes
    nsv6309831copy number variation1nstd102humanUncertain significance GRCh37 chr15: 89,859,982-90,294,462 , GRCh38.p12 chr15: 89,316,751-89,751,231 LOC107984777, PLIN1, 19 more genes
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
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