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Items: 1 to 20 of 336

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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
    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
    nsv7077958inversion1nstd229human GRCh38 chr15: 100,950,908-101,592,405 , GRCh37.p13 chr15: 101,491,113-102,132,608 LOC107984727, LRRK1, 9 more genes
    nsv7075901inversion1nstd229human GRCh38 chr15: 99,795,287-101,786,621 , GRCh37.p13 chr15: 100,335,492-102,326,824 GOLGA8VP, DNM1P46, 39 more genes
    nsv7072319inversion1nstd229human GRCh38 chr15: 99,798,704-101,768,404 , GRCh37.p13 chr15: 100,338,909-102,308,607 ADAMTS17, TARS3, 37 more genes
    nsv7071630inversion1nstd229human GRCh38 chr15: 99,746,792-101,514,499 , GRCh37.p13 chr15: 100,286,997-102,054,702 RN7SL484P, ALDH1A3, 32 more genes
    nsv7059511inversion1nstd229human GRCh38 chr15: 99,784,046-101,789,074 , GRCh37.p13 chr15: 100,324,251-102,329,277 RNA5SP402, TM2D3, 40 more genes
    nsv6973393copy number variation1nstd229human GRCh38 chr15: 101,123,701-101,281,300 , GRCh37.p13 chr15: 101,663,906-101,821,505 LOC105371026, CHSY1, 3 more genes
    nsv6973372copy number variation1nstd229human GRCh38 chr15: 100,746,839-101,592,082 , GRCh37.p13 chr15: 101,287,044-102,132,285 LOC440313, LOC107987228, 15 more genes
    nsv6973042copy number variation1nstd229human GRCh38 chr15: 101,127,371-101,697,216 , GRCh37.p13 chr15: 101,667,576-102,237,419 LOC107987228, CHSY1, 12 more genes
    nsv6968563copy number variation1nstd229human GRCh38 chr15: 101,217,356-101,440,091 , GRCh37.p13 chr15: 101,757,561-101,980,296 SNRPA1, CHSY1, 5 more genes
    nsv6966928copy number variation1nstd229human GRCh38 chr15: 101,182,872-101,351,952 , GRCh37.p13 chr15: 101,723,077-101,892,157 PCSK6, CHSY1, 5 more genes
    nsv6960489copy number variation1nstd229human GRCh38 chr15: 101,254,744-101,284,495 , GRCh37.p13 chr15: 101,794,949-101,824,700 SELENOS, LOC107984727, 1 more genes
    nsv6960141copy number variation1nstd229human GRCh38 chr15: 100,914,020-101,454,399 , GRCh37.p13 chr15: 101,454,225-101,994,604 PCSK6, ALDH1A3, 9 more genes
    nsv6959126copy number variation1nstd229human GRCh38 chr15: 101,284,507-101,472,022 , GRCh37.p13 chr15: 101,824,712-102,012,227 PCSK6-AS1, PCSK6, 2 more genes
    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
    nsv6622767copy number variation1nstd224human GRCh37 chr15: 101,832,180-102,055,559 , GRCh38.p12 chr15: 101,291,975-101,515,356 LOC100507472, PCSK6-AS1, 3 more genes
    nsv6622766copy number variation1nstd224human GRCh37 chr15: 101,561,092-102,069,043 , GRCh38.p12 chr15: 101,020,887-101,528,840 CHSY1, SELENOS, 8 more genes
    nsv6593771inversion1nstd223human GRCh38 chr15: 99,795,890-101,768,715 , GRCh37.p13 chr15: 100,336,095-102,308,918 LOC107987228, SPATA41, 37 more genes
    nsv6591507inversion1nstd223human GRCh38 chr15: 99,791,140-101,782,108 , GRCh37.p13 chr15: 100,331,345-102,322,311 LINS1, SNRPA1, 40 more genes
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