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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7059635inversion1nstd229human GRCh38 chr15: 51,716,761-55,548,818 , GRCh37.p13 chr15: 52,008,958-55,841,016 CCPG1, LOC105370823, 51 more genes
    nsv7059534inversion1nstd229human GRCh38 chr15: 51,726,660-55,605,328 , GRCh37.p13 chr15: 52,018,857-55,897,526 HNRNPA1P74, MYO5C, 50 more genes
    nsv6972468copy number variation1nstd229human GRCh38 chr15: 51,731,623-51,735,035 , GRCh37.p13 chr15: 52,023,820-52,027,232 LYSMD2
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6584870inversion1nstd223human GRCh38 chr15: 51,741,646-51,742,197 , GRCh37.p13 chr15: 52,033,843-52,034,394 LYSMD2
    nsv6576127inversion1nstd223human GRCh38 chr15: 51,729,504-51,730,465 , GRCh37.p13 chr15: 52,021,701-52,022,662 LYSMD2
    nsv6510239copy number variation1nstd223human GRCh38 chr15: 51,732,801-51,762,600 , GRCh37.p13 chr15: 52,024,998-52,054,797 LYSMD2, TMOD2
    nsv6509707copy number variation1nstd223human GRCh38 chr15: 51,738,901-51,751,400 , GRCh37.p13 chr15: 52,031,098-52,043,597 LYSMD2, TMOD2
    nsv6503279copy number variation1nstd223human GRCh38 chr15: 51,728,201-51,762,100 , GRCh37.p13 chr15: 52,020,398-52,054,297 TMOD2, LYSMD2
    nsv6501548copy number variation1nstd223human GRCh38 chr15: 51,731,623-51,735,031 , GRCh37.p13 chr15: 52,023,820-52,027,228 LYSMD2
    nsv6500722copy number variation1nstd223human GRCh38 chr15: 51,721,031-51,730,778 , GRCh37.p13 chr15: 52,013,228-52,022,975 SCG3, LYSMD2
    nsv6500220copy number variation1nstd223human GRCh38 chr15: 51,721,701-51,723,100 , GRCh37.p13 chr15: 52,013,898-52,015,297 LYSMD2
    nsv6499439copy number variation1nstd223human GRCh38 chr15: 51,731,865-51,732,496 , GRCh37.p13 chr15: 52,024,062-52,024,693 LYSMD2
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6290450copy number variation1nstd102humanUncertain significance GRCh38 chr15: 51,681,311-51,791,472 , GRCh37.p13 chr15: 51,973,508-52,083,669 TMOD2, SCG3, 1 more genes
    nsv6132897copy number variation1nstd213human GRCh37 chr15: 50,000,000-53,730,001 , GRCh38.p12 chr15: 49,707,803-53,437,804 MAPK6, ARPP19, 65 more genes
    nsv5978551insertion1nstd209human GRCh38 chr15: 51,748,288-51,748,288 , GRCh37.p13 chr15: 52,040,485-52,040,485 LYSMD2
    nsv5934918copy number variation1nstd209human GRCh38 chr15: 51,747,141-51,747,431 , GRCh37.p13 chr15: 52,039,338-52,039,628 LYSMD2
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