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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6996870copy number variation1nstd229human GRCh38 chr17: 81,522,040-81,556,823 , GRCh37.p13 chr17: 79,498,448-79,523,849 FAAP100, NPLOC4, 1 more genes
    nsv6993349copy number variation1nstd229human GRCh38 chr17: 81,541,764-81,566,778 , GRCh37.p13 chr17: 79,508,790-79,533,804 FAAP100, NPLOC4
    nsv6986155copy number variation1nstd229human GRCh38 chr17: 81,536,790-81,597,744 , GRCh37.p13 chr17: 79,503,816-79,564,770 NPLOC4, FAAP100, 1 more genes
    nsv6624126copy number variation1nstd224human GRCh37 chr17: 79,511,135-79,532,654 , GRCh38.p12 chr17: 81,544,109-81,565,628 FAAP100, NPLOC4
    nsv6534585copy number variation1nstd223human GRCh38 chr17: 81,541,764-81,566,776 , GRCh37.p13 chr17: 79,508,790-79,533,802 FAAP100, NPLOC4
    nsv6531674copy number variation1nstd223human GRCh38 chr17: 81,538,842-81,539,185 , GRCh37.p13 chr17: 79,505,868-79,506,211 FAAP100
    nsv6525877copy number variation1nstd223human GRCh38 chr17: 81,477,998-81,555,207 , GRCh37.p13 chr17|NW_003871087.1: 132,636-186,059 , GRCh37.p13 chr17: 79,445,024-79,498,447 NPLOC4, LINC01971, 3 more genes
    nsv6524408copy number variation1nstd223human GRCh38 chr17: 81,528,040-81,550,054 , GRCh37.p13 chr17: 79,498,448-79,517,080 FAAP100, FSCN2
    nsv6523616copy number variation1nstd223human GRCh38 chr17: 81,548,707-81,555,100 , GRCh37.p13 chr17: 79,515,733-79,522,126 NPLOC4, FAAP100
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6259116mobile element insertion1nstd215human GRCh38 chr17: 81,542,201-81,542,201 , GRCh37.p13 chr17: 79,509,227-79,509,227 FAAP100
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv5708403mobile element insertion1nstd211human GRCh38 chr17: 81,542,201-81,542,201 , GRCh37.p13 chr17: 79,509,227-79,509,227 FAAP100
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5294695copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-81,587,000 , GRCh37.p13 chr17: 78,904,301-79,554,026 , LOC105371926, 32 more genes
    nsv5142066mobile element insertion1nstd203human GRCh38 chr17: 81,542,201-81,542,210 , GRCh37.p13 chr17: 79,509,227-79,509,236 FAAP100
    nsv5017044copy number variation1nstd200human GRCh38 chr17: 81,441,456-81,816,579 , GRCh37.p13 chr17: 79,498,418-79,774,455 , LOC105376789, 19 more genes
    nsv5014116copy number variation1nstd200human GRCh38 chr17: 81,541,764-81,566,778 , GRCh37.p13 chr17: 79,508,790-79,533,804 FAAP100, NPLOC4
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