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Items: 1 to 20 of 175

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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
    nsv7073585inversion1nstd229human GRCh38 chr15: 52,093,790-52,249,452 , GRCh37.p13 chr15: 52,385,987-52,541,649 GNB5, BCL2L10, 5 more genes
    nsv7065803inversion1nstd229human GRCh38 chr15: 52,155,809-52,383,429 , GRCh37.p13 chr15: 52,448,006-52,675,626 LOC105370820, GNB5, 5 more genes
    nsv7065242inversion1nstd229human GRCh38 chr15: 52,093,673-52,247,548 , GRCh37.p13 chr15: 52,385,870-52,539,745 BCL2L10, CERNA1, 5 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
    nsv6976841copy number variation1nstd229human GRCh38 chr15: 52,202,811-52,202,889 , GRCh37.p13 chr15: 52,495,008-52,495,086 MYO5C, CERNA1
    nsv6974313copy number variation1nstd229human GRCh38 chr15: 52,068,601-52,324,700 , GRCh37.p13 chr15: 52,360,798-52,616,897 RPS13P8, LOC112268150, 8 more genes
    nsv6973598copy number variation1nstd229human GRCh38 chr15: 52,155,801-52,460,300 , GRCh37.p13 chr15: 52,447,998-52,752,497 MIR1266, LOC105370819, 5 more genes
    nsv6968212copy number variation1nstd229human GRCh38 chr15: 52,193,801-52,204,800 , GRCh37.p13 chr15: 52,485,998-52,496,997 CERNA1, MYO5C
    nsv6966374copy number variation1nstd229human GRCh38 chr15: 52,082,901-52,181,000 , GRCh37.p13 chr15: 52,375,098-52,473,197 LOC112268150, BCL2L10, 3 more genes
    nsv6965961copy number variation1nstd229human GRCh38 chr15: 52,195,311-52,195,608 , GRCh37.p13 chr15: 52,487,508-52,487,805 MYO5C, CERNA1
    nsv6964268copy number variation1nstd229human GRCh38 chr15: 52,170,738-52,182,143 , GRCh37.p13 chr15: 52,462,935-52,474,340 CERNA1, GNB5
    nsv6963536copy number variation1nstd229human GRCh38 chr15: 52,132,106-52,235,750 , GRCh37.p13 chr15: 52,424,303-52,527,947 MYO5C, GNB5, 2 more genes
    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
    nsv6592253inversion1nstd223human GRCh38 chr15: 52,189,316-52,190,192 , GRCh37.p13 chr15: 52,481,513-52,482,389 CERNA1, GNB5
    nsv6512874copy number variation1nstd223human GRCh38 chr15: 52,190,353-52,198,816 , GRCh37.p13 chr15: 52,482,550-52,491,013 MYO5C, CERNA1, 1 more genes
    nsv6511419copy number variation1nstd223human GRCh38 chr15: 52,202,368-52,207,085 , GRCh37.p13 chr15: 52,494,565-52,499,282 CERNA1, MYO5C
    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
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