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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7095147copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850 SLC35G3, AP2B1, 26 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6996891copy number variation1nstd229human GRCh38 chr17: 35,353,501-35,441,800 , GRCh37.p13 chr17: 33,680,520-33,768,819 LOC729839, SLFN12, 4 more genes
    nsv6994838copy number variation1nstd229human GRCh38 chr17: 35,170,807-35,536,994 , GRCh37.p13 chr17: 33,497,826-33,864,013 SLFN5, SPICP2, 15 more genes
    nsv6993239copy number variation1nstd229human GRCh38 chr17: 35,167,502-35,536,993 , GRCh37.p13 chr17: 33,494,521-33,864,012 LOC105371932, SLC35G3, 15 more genes
    nsv6989897copy number variation1nstd229human GRCh38 chr17: 35,444,911-35,448,271 , GRCh37.p13 chr17: 33,771,930-33,775,290 SLFN13
    nsv6985797copy number variation1nstd229human GRCh38 chr17: 35,353,001-35,441,600 , GRCh37.p13 chr17: 33,680,020-33,768,619 LOC729839, LOC105371933, 4 more genes
    nsv6983798copy number variation1nstd229human GRCh38 chr17: 35,440,961-35,448,266 , GRCh37.p13 chr17: 33,767,980-33,775,285 SLFN13
    nsv6983643copy number variation1nstd229human GRCh38 chr17: 35,440,960-35,444,849 , GRCh37.p13 chr17: 33,767,979-33,771,868 SLFN13
    nsv6982202copy number variation1nstd229human GRCh38 chr17: 34,998,758-35,727,529 , GRCh37.p13 chr17: 33,325,777-34,034,851 SLFN11, LOC105371932, 32 more genes
    nsv6981859copy number variation1nstd229human GRCh38 chr17: 35,342,081-35,441,375 , GRCh37.p13 chr17: 33,669,100-33,768,394 SLFN13, UFM1P2, 5 more genes
    nsv6980165copy number variation1nstd229human GRCh38 chr17: 35,353,701-35,441,900 , GRCh37.p13 chr17: 33,680,720-33,768,919 LOC729839, LOC105371933, 4 more genes
    nsv6635418copy number variation1nstd227human GRCh37 chr17: 33,684,035-33,768,199 , GRCh38.p12 chr17: 35,357,016-35,441,180 SLFN12, SLFN11, 4 more genes
    nsv6634448copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,756,756-34,005,513 , GRCh38.p12 chr17: 35,429,737-35,678,494 LOC100420062, TAF5LP1, 13 more genes
    nsv6624270copy number variation1nstd224human GRCh37 chr17: 33,680,941-33,769,211 , GRCh38.p12 chr17: 35,353,922-35,442,192 SLFN12, SLFN11, 4 more genes
    nsv6624269copy number variation7nstd224human GRCh37 chr17: 33,680,941-33,768,284 , GRCh38.p12 chr17: 35,353,922-35,441,265 SLFN12, SLFN11, 4 more genes
    nsv6624227copy number variation5nstd224human GRCh37 chr17: 33,680,941-33,768,368 , GRCh38.p12 chr17: 35,353,922-35,441,349 SLFN12, SLFN11, 4 more genes
    nsv6624074copy number variation1nstd224human GRCh37 chr17: 33,682,734-33,768,601 , GRCh38.p12 chr17: 35,355,715-35,441,582 SLFN12, SLFN11, 4 more genes
    nsv6624073copy number variation6nstd224human GRCh37 chr17: 33,682,734-33,766,040 , GRCh38.p12 chr17: 35,355,715-35,439,021 SLFN12, SLFN11, 4 more genes
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