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Items: 1 to 20 of 388

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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
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7076478inversion1nstd229human GRCh38 chr15: 79,261,836-81,280,491 , GRCh37.p13 chr15: 79,554,178-81,572,832 CFAP161, TMED3, 34 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6977031copy number variation1nstd229human GRCh38 chr15: 79,444,901-79,449,900 , GRCh37.p13 chr15: 79,737,243-79,742,242 MINAR1
    nsv6976337copy number variation1nstd229human GRCh38 chr15: 79,458,834-79,465,475 , GRCh37.p13 chr15: 79,751,176-79,757,817 MINAR1, LOC105370918
    nsv6975659copy number variation1nstd229human GRCh38 chr15: 79,461,229-79,545,622 , GRCh37.p13 chr15: 79,753,571-79,837,964 LOC105370919, MINAR1, 1 more genes
    nsv6975341copy number variation1nstd229human GRCh38 chr15: 79,444,412-79,448,744 , GRCh37.p13 chr15: 79,736,754-79,741,086 MINAR1
    nsv6974774copy number variation1nstd229human GRCh38 chr15: 79,246,961-80,113,369 , GRCh37.p13 chr15: 79,539,303-80,405,711 ST20-AS1, RNU6-667P, 17 more genes
    nsv6969140copy number variation1nstd229human GRCh38 chr15: 79,401,001-79,411,100 , GRCh37.p13 chr15: 79,693,343-79,703,442 MINAR1, TMED3
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6967220copy number variation1nstd229human GRCh38 chr15: 79,425,710-79,429,208 , GRCh37.p13 chr15: 79,718,052-79,721,550 MINAR1
    nsv6966757copy number variation1nstd229human GRCh38 chr15: 79,366,350-79,430,733 , GRCh37.p13 chr15: 79,658,692-79,723,075 MINAR1, TMED3
    nsv6964920copy number variation1nstd229human GRCh38 chr15: 79,423,498-79,428,107 , GRCh37.p13 chr15: 79,715,840-79,720,449 MINAR1
    nsv6960238copy number variation1nstd229human GRCh38 chr15: 79,457,444-79,469,657 , GRCh37.p13 chr15: 79,749,786-79,761,999 LOC105370918, MINAR1
    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
    nsv6623285copy number variation1nstd224human GRCh37 chr15: 79,658,995-79,711,390 , GRCh38.p12 chr15: 79,366,653-79,419,048 TMED3, MINAR1
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