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Items: 1 to 20 of 273

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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
    nsv7076849inversion1nstd229human GRCh38 chr15: 89,041,443-89,639,935 , GRCh37.p13 chr15: 89,584,674-90,183,166 LINC00928, HMGB1P8, 17 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
    nsv6975790copy number variation1nstd229human GRCh38 chr15: 89,529,948-89,676,537 , GRCh37.p13 chr15: 90,073,179-90,219,768 KIF7, TICRR, 1 more genes
    nsv6972391copy number variation1nstd229human GRCh38 chr15: 89,591,988-89,619,290 , GRCh37.p13 chr15: 90,135,219-90,162,521 TICRR
    nsv6971076copy number variation1nstd229human GRCh38 chr15: 89,613,141-89,651,334 , GRCh37.p13 chr15: 90,156,372-90,194,565 TICRR, KIF7
    nsv6965793copy number variation1nstd229human GRCh38 chr15: 89,587,407-89,592,470 , GRCh37.p13 chr15: 90,130,638-90,135,701 TICRR
    nsv6965360copy number variation1nstd229human GRCh38 chr15: 89,576,830-89,581,780 , GRCh37.p13 chr15: 90,120,061-90,125,011 TICRR
    nsv6961795copy number variation1nstd229human GRCh38 chr15: 89,574,410-89,574,579 , GRCh37.p13 chr15: 90,117,641-90,117,810 TICRR
    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
    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
    nsv6589108inversion1nstd223human GRCh38 chr15: 89,618,843-89,619,342 , GRCh37.p13 chr15: 90,162,074-90,162,573 TICRR
    nsv6588169inversion1nstd223human GRCh38 chr15: 89,596,358-89,597,530 , GRCh37.p13 chr15: 90,139,589-90,140,761 TICRR
    nsv6587966inversion1nstd223human GRCh38 chr15: 89,598,337-89,599,028 , GRCh37.p13 chr15: 90,141,568-90,142,259 TICRR
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