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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7077206inversion1nstd229human GRCh38 chr15: 69,695,373-69,695,411 , GRCh37.p13 chr15: 69,987,712-69,987,750 PCAT29
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv6975900copy number variation1nstd229human GRCh38 chr15: 69,609,395-69,616,087 , GRCh37.p13 chr15: 69,901,734-69,908,426 PCAT29
    nsv6973965copy number variation1nstd229human GRCh38 chr15: 69,276,390-69,590,208 , GRCh37.p13 chr15: 69,568,729-69,882,547 KIF23-AS1, KIF23, 7 more genes
    nsv6970838copy number variation1nstd229human GRCh38 chr15: 69,602,927-69,605,919 , GRCh37.p13 chr15: 69,895,266-69,898,258 PCAT29
    nsv6968623copy number variation1nstd229human GRCh38 chr15: 69,681,733-69,694,120 , GRCh37.p13 chr15: 69,974,072-69,986,459 PCAT29
    nsv6966998copy number variation1nstd229human GRCh38 chr15: 69,637,435-69,640,612 , GRCh37.p13 chr15: 69,929,774-69,932,951 PCAT29
    nsv6964847copy number variation1nstd229human GRCh38 chr15: 69,631,999-69,632,054 , GRCh37.p13 chr15: 69,924,338-69,924,393 PCAT29
    nsv6963887copy number variation1nstd229human GRCh38 chr15: 69,654,521-69,661,817 , GRCh37.p13 chr15: 69,946,860-69,954,156 PCAT29
    nsv6963679copy number variation1nstd229human GRCh38 chr15: 69,624,062-69,624,411 , GRCh37.p13 chr15: 69,916,401-69,916,750 PCAT29
    nsv6961511copy number variation1nstd229human GRCh38 chr15: 69,587,698-69,593,794 , GRCh37.p13 chr15: 69,880,037-69,886,133 PCAT29
    nsv6960818copy number variation1nstd229human GRCh38 chr15: 69,670,042-69,674,477 , GRCh37.p13 chr15: 69,962,381-69,966,816 PCAT29
    nsv6960172copy number variation1nstd229human GRCh38 chr15: 69,684,217-69,686,778 , GRCh37.p13 chr15: 69,976,556-69,979,117 PCAT29
    nsv6637906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 68,807,665-70,981,473 , GRCh38.p12 chr15: 68,515,326-70,689,134 UACA, RPLP1, 36 more genes
    nsv6586978inversion1nstd223human GRCh38 chr15: 69,688,038-69,688,858 , GRCh37.p13 chr15: 69,980,377-69,981,197 PCAT29
    nsv6515250copy number variation1nstd223human GRCh38 chr15: 69,645,469-69,649,096 , GRCh37.p13 chr15: 69,937,808-69,941,435 PCAT29
    nsv6510232copy number variation1nstd223human GRCh38 chr15: 69,614,001-69,616,600 , GRCh37.p13 chr15: 69,906,340-69,908,939 PCAT29
    nsv6507804copy number variation1nstd223human GRCh38 chr15: 69,674,621-69,675,250 , GRCh37.p13 chr15: 69,966,960-69,967,589 PCAT29
    nsv6287500insertion1nstd214human GRCh38 chr15: 69,696,159-69,696,159 , GRCh37.p13 chr15: 69,988,498-69,988,498 PCAT29
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