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Items: 1 to 20 of 218

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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
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 LOC105370892, MRPS15P1, 99 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
    nsv7094733copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,628,431-76,054,677 , GRCh38.p12 chr15: 75,336,090-75,762,336 LOC101929408, MAN2C1, 16 more genes
    nsv7077484inversion1nstd229human GRCh38 chr15: 74,072,224-75,785,570 , GRCh37.p13 chr15: 74,364,565-76,077,911 LOC107984720, SCAMP2, 68 more genes
    nsv7077374inversion1nstd229human GRCh38 chr15: 74,978,016-75,592,041 , GRCh37.p13 chr15: 75,270,357-75,884,382 PPCDC, RPL13P4, 21 more genes
    nsv7075916inversion1nstd229human GRCh38 chr15: 75,241,707-77,965,147 , GRCh37.p13 chr15: 75,534,048-78,257,489 PTPN9, LOC105370902, 60 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 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
    nsv7059590inversion1nstd229human GRCh38 chr15: 75,219,584-75,775,597 , GRCh37.p13 chr15: 75,511,925-76,067,938 LOC107984720, MIR631, 25 more genes
    nsv6976129copy number variation1nstd229human GRCh38 chr15: 75,339,333-75,474,591 , GRCh37.p13 chr15: 75,631,674-75,766,932 SIN3A, COMMD4, 6 more genes
    nsv6973977copy number variation1nstd229human GRCh38 chr15: 75,358,564-75,361,599 , GRCh37.p13 chr15: 75,650,905-75,653,940 MAN2C1
    nsv6959706copy number variation1nstd229human GRCh38 chr15: 75,355,455-75,355,506 , GRCh37.p13 chr15: 75,647,796-75,647,847 NEIL1, MAN2C1
    nsv6637477copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055 PTPN9, NRG4, 96 more genes
    nsv6623336copy number variation1nstd224human GRCh37 chr15: 75,641,367-75,654,685 , GRCh38.p12 chr15: 75,349,026-75,362,344 MAN2C1, NEIL1, 1 more genes
    nsv6589853inversion1nstd223human GRCh38 chr15: 75,227,742-75,760,512 , GRCh37.p13 chr15: 75,520,083-76,052,853 SNX33, LOC101929408, 24 more genes
    nsv6588320inversion1nstd223human GRCh38 chr15: 75,225,241-75,762,978 , GRCh37.p13 chr15: 75,517,582-76,055,319 NEIL1, DNM1P35, 24 more genes
    nsv6582103inversion1nstd223human GRCh38 chr15: 75,332,358-77,947,953 , GRCh37.p13 chr15: 75,624,699-78,240,295 DNM1P9, TSPAN3, 53 more genes
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