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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7045904inversion1nstd229human GRCh38 chr1: 236,415,671-241,161,975 , GRCh37.p13 chr1: 236,578,971-241,325,275 PSMD2P1, RN7SKP195, 55 more genes
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv6673173copy number variation1nstd229human GRCh38 chr1: 236,398,540-236,555,370 , GRCh37.p13 chr1: 236,561,840-236,718,670 ENO1P1, HEATR1, 3 more genes
    nsv6670408copy number variation1nstd229human GRCh38 chr1: 236,523,401-236,526,000 , GRCh37.p13 chr1: 236,686,701-236,689,300 LGALS8, LGALS8-AS1
    nsv6669086copy number variation1nstd229human GRCh38 chr1: 236,178,821-236,566,887 , GRCh37.p13 chr1: 236,342,121-236,730,187 LGALS8, LGALS8-AS1, 7 more genes
    nsv6662257copy number variation1nstd229human GRCh38 chr1: 236,253,901-236,547,900 , GRCh37.p13 chr1: 236,417,201-236,711,200 HEATR1, LOC100130485, 6 more genes
    nsv6661754copy number variation1nstd229human GRCh38 chr1: 236,182,764-236,747,255 , GRCh37.p13 chr1: 236,346,064-236,910,555 HEATR1, RNU2-70P, 8 more genes
    nsv6659207copy number variation1nstd229human GRCh38 chr1: 236,473,473-236,544,347 , GRCh37.p13 chr1: 236,636,773-236,707,647 LGALS8-AS1, EDARADD, 2 more genes
    nsv6658563copy number variation1nstd229human GRCh38 chr1: 236,523,753-236,532,958 , GRCh37.p13 chr1: 236,687,053-236,696,258 LGALS8, LGALS8-AS1
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636217copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914 LINC01347, LOC100130331, 169 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 OR2M4, KIF28P, 316 more genes
    nsv6332204copy number variation1nstd223human GRCh38 chr1: 236,500,299-236,522,413 , GRCh37.p13 chr1: 236,663,599-236,685,713 LGALS8-AS1, LGALS8
    nsv6330446copy number variation1nstd223human GRCh38 chr1: 236,398,540-236,555,370 , GRCh37.p13 chr1: 236,561,840-236,718,670 HEATR1, LGALS8, 3 more genes
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