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Items: 1 to 20 of 693

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142437copy number variation1nstd232human GRCh37.p13 chr15: 68,063,458-68,063,513 , GRCh38.p12 chr15: 67,771,120-67,771,175 MAP2K5
    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
    nsv7077995inversion1nstd229human GRCh38 chr15: 67,715,225-67,719,431 , GRCh37.p13 chr15: 68,007,563-68,011,769 MAP2K5
    nsv7072982inversion1nstd229human GRCh38 chr15: 67,621,376-67,621,423 , GRCh37.p13 chr15: 67,913,714-67,913,761 MAP2K5
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7066684inversion1nstd229human GRCh38 chr15: 67,645,727-67,661,893 , GRCh37.p13 chr15: 67,938,065-67,954,231 MAP2K5
    nsv7064423inversion1nstd229human GRCh38 chr15: 67,680,322-67,680,390 , GRCh37.p13 chr15: 67,972,660-67,972,728 MAP2K5
    nsv6977259copy number variation1nstd229human GRCh38 chr15: 67,784,594-67,789,471 , GRCh37.p13 chr15: 68,076,932-68,081,809 MAP2K5
    nsv6976719copy number variation1nstd229human GRCh38 chr15: 67,716,447-67,718,223 , GRCh37.p13 chr15: 68,008,785-68,010,561 MAP2K5
    nsv6975806copy number variation1nstd229human GRCh38 chr15: 67,649,804-67,656,144 , GRCh37.p13 chr15: 67,942,142-67,948,482 MAP2K5
    nsv6974923copy number variation1nstd229human GRCh38 chr15: 67,802,201-67,806,300 , GRCh37.p13 chr15: 68,094,539-68,098,638 MAP2K5
    nsv6974166copy number variation1nstd229human GRCh38 chr15: 67,595,488-67,595,692 , GRCh37.p13 chr15: 67,887,826-67,888,030 MAP2K5
    nsv6974054copy number variation1nstd229human GRCh38 chr15: 67,579,708-67,579,738 , GRCh37.p13 chr15: 67,872,046-67,872,076 MAP2K5
    nsv6974001copy number variation1nstd229human GRCh38 chr15: 67,545,751-67,548,098 , GRCh37.p13 chr15: 67,838,089-67,840,436 MAP2K5
    nsv6973139copy number variation1nstd229human GRCh38 chr15: 67,705,219-67,710,721 , GRCh37.p13 chr15: 67,997,557-68,003,059 MAP2K5
    nsv6973069copy number variation1nstd229human GRCh38 chr15: 67,800,104-67,800,265 , GRCh37.p13 chr15: 68,092,442-68,092,603 MAP2K5
    nsv6971057copy number variation1nstd229human GRCh38 chr15: 67,781,037-67,814,769 , GRCh37.p13 chr15: 68,073,375-68,107,107 MAP2K5
    nsv6970812copy number variation1nstd229human GRCh38 chr15: 67,615,703-67,615,731 , GRCh37.p13 chr15: 67,908,041-67,908,069 MAP2K5
    nsv6970448copy number variation1nstd229human GRCh38 chr15: 67,681,322-67,684,468 , GRCh37.p13 chr15: 67,973,660-67,976,806 MAP2K5
    nsv6970303copy number variation1nstd229human GRCh38 chr15: 67,585,980-67,590,232 , GRCh37.p13 chr15: 67,878,318-67,882,570 MAP2K5
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