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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055819inversion1nstd229human GRCh37.p13 chr7|NW_003571037.1: 152,792-312,266 , GRCh38 chr7: 102,228,462-102,387,936 , GRCh37.p13 chr7: 101,871,742-102,028,383 LOC100289561, SH2B2, 6 more genes
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7052662inversion1nstd229human GRCh38 chr7: 102,309,147-103,483,817 , GRCh37.p13 chr7: 102,072,448-103,124,264 S100A11P1, RPL7AP39, 46 more genes
    nsv7040420inversion1nstd229human GRCh38 chr7: 101,445,712-104,173,878 , GRCh37.p13 chr7: 101,088,993-103,814,326 ALKBH4, RPS29P16, 54 more genes
    nsv6834007copy number variation1nstd229human GRCh38 chr7: 102,380,701-102,384,900 , GRCh37.p13 chr7|NW_003571037.1: 305,031-309,230 , GRCh37.p13 chr7: 102,021,148-102,025,347 LOC100630923, LOC100289561
    nsv6830791copy number variation1nstd229human GRCh38 chr7: 102,369,213-102,369,428 , GRCh37.p13 chr7|NW_003571037.1: 293,543-293,758 , GRCh37.p13 chr7: 102,009,660-102,009,875 LOC100289561, LOC100630923
    nsv6818476copy number variation1nstd229human GRCh38 chr7: 102,321,437-102,410,929 , GRCh37.p13 chr7|NW_003571037.1: 245,767-335,259 , GRCh37.p13 chr7: 101,961,904-102,051,376 SH2B2, SPDYE6, 7 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631801copy number variation1nstd224human GRCh37 chr7: 101,957,816-102,114,090 , GRCh38.p12 chr7: 102,317,349-102,473,643 ALKBH4, LOC100630923, 13 more genes
    nsv6631293copy number variation1nstd224human GRCh37 chr7: 101,870,948-102,113,373 , GRCh38.p12 chr7: 102,227,668-102,472,926 CUX1, ALKBH4, 15 more genes
    nsv6617867copy number variation1nstd223human GRCh38 chr7: 102,327,148-102,380,454 , GRCh37.p13 chr7: 101,967,566-102,020,901 , GRCh37.p13 chr7|NW_003571037.1: 251,478-304,784 LOC107986717, SPDYE6, 3 more genes
    nsv6602521copy number variation1nstd223human GRCh38 chr7: 102,167,380-103,063,308 , GRCh37.p13 chr7: 102,072,448-102,703,755 MIR4467, MIR548O, 32 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6291301copy number variation1nstd102humanUncertain significance GRCh37 chr7: 101,729,998-102,114,340 , GRCh38.p12 chr7: 102,086,718-102,473,893 LOC105375433, CUX1, 15 more genes
    nsv6283951insertion1nstd214human GRCh37.p13 chr7|NW_003571037.1: 293,773-293,773 , GRCh38 chr7: 102,369,443-102,369,443 , GRCh37.p13 chr7: 102,009,890-102,009,890 LOC100289561, LOC100630923
    nsv6184033copy number variation1nstd214human GRCh38 chr7: 102,369,006-102,369,067 , GRCh37.p13 chr7|NW_003571037.1: 293,336-293,397 , GRCh37.p13 chr7: 102,009,453-102,009,514 LOC100289561, LOC100630923
    nsv6141707copy number variation1nstd206human GRCh37.p13 chr7|NW_003571037.1: 253,109-307,109 , GRCh38 chr7: 102,328,779-102,382,779 , GRCh37.p13 chr7: 101,969,196-102,023,226 PMS2P12, LOC100289561, 3 more genes
    nsv6136532copy number variation1nstd213human GRCh37 chr7: 101,870,000-102,140,001 , GRCh38.p12 chr7: 102,226,720-102,499,554 LRWD1, LOC100289561, 16 more genes
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