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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
    nsv7070157inversion1nstd229human GRCh38 chr15: 79,995,616-80,097,328 , GRCh37.p13 chr15: 80,287,958-80,389,670 ZFAND6
    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
    nsv6976481copy number variation1nstd229human GRCh38 chr15: 80,088,799-80,093,335 , GRCh37.p13 chr15: 80,381,141-80,385,677 ZFAND6
    nsv6976388copy number variation1nstd229human GRCh38 chr15: 80,099,011-80,101,486 , GRCh37.p13 chr15: 80,391,353-80,393,828 ZFAND6
    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
    nsv6971626copy number variation1nstd229human GRCh38 chr15: 80,134,377-80,141,620 , GRCh37.p13 chr15: 80,426,719-80,433,962 ZFAND6
    nsv6970861copy number variation1nstd229human GRCh38 chr15: 80,084,178-80,087,124 , GRCh37.p13 chr15: 80,376,520-80,379,466 ZFAND6
    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
    nsv6967870copy number variation1nstd229human GRCh38 chr15: 80,104,561-80,116,009 , GRCh37.p13 chr15: 80,396,903-80,408,351 ZFAND6
    nsv6960305copy number variation1nstd229human GRCh38 chr15: 80,063,422-80,065,577 , GRCh37.p13 chr15: 80,355,764-80,357,919 ZFAND6
    nsv6959756copy number variation1nstd229human GRCh38 chr15: 80,130,451-80,130,730 , GRCh37.p13 chr15: 80,422,793-80,423,072 ZFAND6
    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
    nsv6637608copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,996,626-82,097,796 , GRCh38.p12 chr15: 79,704,284-81,805,455 ARNT2, LOC105370921, 31 more genes
    nsv6623338copy number variation1nstd224human GRCh37 chr15: 80,293,439-80,432,222 , GRCh38.p12 chr15: 80,001,097-80,139,880 ZFAND6
    nsv6594439inversion1nstd223human GRCh38 chr15: 80,092,978-80,093,665 , GRCh37.p13 chr15: 80,385,320-80,386,007 ZFAND6
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