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Items: 1 to 20 of 178

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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
    nsv7094317copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,489,824-91,496,946 , GRCh38.p12 chr15: 90,946,594-90,953,716 UNC45A, RCCD1
    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
    nsv7093404copy number variation1nstd102humannot provided GRCh37 chr15: 91,422,650-91,497,515 , GRCh38.p12 chr15: 90,879,420-90,954,285 FURIN, RCCD1, 4 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
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6976150copy number variation1nstd229human GRCh38 chr15: 90,790,101-90,986,300 , GRCh37.p13 chr15: 91,333,331-91,529,530 UNC45A, MAN2A2, 9 more genes
    nsv6969933copy number variation1nstd229human GRCh38 chr15: 90,946,031-90,958,117 , GRCh37.p13 chr15: 91,489,261-91,501,347 RCCD1, UNC45A
    nsv6962202copy number variation1nstd229human GRCh38 chr15: 90,873,702-90,968,294 , GRCh37.p13 chr15: 91,416,932-91,511,524 UNC45A, MAN2A2, 6 more genes
    nsv6958791copy number variation1nstd229human GRCh38 chr15: 90,959,868-90,959,954 , GRCh37.p13 chr15: 91,503,098-91,503,184 RCCD1
    nsv6958606copy number variation1nstd229human GRCh38 chr15: 90,955,110-90,955,143 , GRCh37.p13 chr15: 91,498,340-91,498,373 RCCD1
    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
    nsv6623293copy number variation1nstd224human GRCh37 chr15: 91,484,259-91,609,153 , GRCh38.p12 chr15: 90,941,029-91,065,923 PRC1, VPS33B, 6 more genes
    nsv6509334copy number variation1nstd223human GRCh38 chr15: 90,946,029-90,958,116 , GRCh37.p13 chr15: 91,489,259-91,501,346 RCCD1, UNC45A
    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
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6285417insertion1nstd214human GRCh38 chr15: 90,957,148-90,957,148 , GRCh37.p13 chr15: 91,500,378-91,500,378 RCCD1
    nsv6249941mobile element insertion1nstd215human GRCh38 chr15: 90,964,822-90,964,822 , GRCh37.p13 chr15: 91,508,052-91,508,052 PRC1, RCCD1, 1 more genes
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