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Items: 1 to 20 of 966

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7076783inversion1nstd229human GRCh38 chr10: 115,941,137-115,947,054 , GRCh37.p13 chr10|NW_004775432.1: 914,602-920,519 , GRCh37.p13 chr10: 117,700,648-117,706,565 ATRNL1
    nsv7075213inversion1nstd229human GRCh38 chr10: 115,340,843-115,340,859 , GRCh37.p13 chr10|NW_004775432.1: 314,307-314,323 , GRCh37.p13 chr10: 117,100,353-117,100,369 ATRNL1
    nsv7074998inversion1nstd229human GRCh38 chr10: 115,483,914-115,486,428 , GRCh37.p13 chr10|NW_004775432.1: 457,378-459,892 , GRCh37.p13 chr10: 117,243,424-117,245,938 ATRNL1
    nsv7074533inversion1nstd229human GRCh38 chr10: 115,485,439-115,489,136 , GRCh37.p13 chr10|NW_004775432.1: 458,903-462,600 , GRCh37.p13 chr10: 117,244,949-117,248,646 ATRNL1
    nsv7074021inversion1nstd229human GRCh38 chr10: 115,483,976-115,486,431 , GRCh37.p13 chr10|NW_004775432.1: 457,440-459,895 , GRCh37.p13 chr10: 117,243,486-117,245,941 ATRNL1
    nsv7070465inversion1nstd229human GRCh38 chr10: 115,876,603-115,894,953 , GRCh37.p13 chr10: 117,636,114-117,654,464 , GRCh37.p13 chr10|NW_004775432.1: 850,068-868,418 ATRNL1
    nsv7069910inversion1nstd229human GRCh38 chr10: 115,876,621-115,890,557 , GRCh37.p13 chr10|NW_004775432.1: 850,086-864,022 , GRCh37.p13 chr10: 117,636,132-117,650,068 ATRNL1
    nsv7069239inversion1nstd229human GRCh38 chr10: 115,411,164-115,411,200 , GRCh37.p13 chr10|NW_004775432.1: 384,628-384,664 , GRCh37.p13 chr10: 117,170,674-117,170,710 ATRNL1
    nsv7067449inversion1nstd229human GRCh38 chr10: 115,382,161-115,384,742 , GRCh37.p13 chr10: 117,141,671-117,144,252 , GRCh37.p13 chr10|NW_004775432.1: 355,625-358,206 ATRNL1
    nsv7066986inversion1nstd229human GRCh38 chr10: 115,486,485-115,488,981 , GRCh37.p13 chr10|NW_004775432.1: 459,949-462,445 , GRCh37.p13 chr10: 117,245,995-117,248,491 ATRNL1
    nsv7066699inversion1nstd229human GRCh38 chr10: 115,810,024-115,828,314 , GRCh37.p13 chr10|NW_004775432.1: 783,489-801,779 , GRCh37.p13 chr10: 117,569,535-117,587,825 NTAN1P1, ATRNL1
    nsv7064030inversion1nstd229human GRCh38 chr10: 115,921,314-115,921,357 , GRCh37.p13 chr10|NW_004775432.1: 894,779-894,822 , GRCh37.p13 chr10: 117,680,825-117,680,868 ATRNL1, LOC105378497
    nsv7062418inversion1nstd229human GRCh38 chr10: 115,456,193-115,581,870 , GRCh37.p13 chr10|NW_004775432.1: 429,657-555,334 , GRCh37.p13 chr10: 117,215,703-117,341,380 ATRNL1
    nsv7061687inversion1nstd229human GRCh38 chr10: 115,703,660-115,703,673 , GRCh37.p13 chr10|NW_004775432.1: 677,124-677,137 , GRCh37.p13 chr10: 117,463,170-117,463,183 ATRNL1
    nsv7061275inversion1nstd229human GRCh38 chr10: 115,339,767-115,518,420 , GRCh37.p13 chr10|NW_004775432.1: 313,231-491,884 , GRCh37.p13 chr10: 117,099,277-117,277,930 ATRNL1
    nsv7060991inversion1nstd229human GRCh38 chr10: 115,360,519-115,680,820 , GRCh37.p13 chr10|NW_004775432.1: 333,983-654,284 , GRCh37.p13 chr10: 117,120,029-117,440,330 ATRNL1
    nsv6898050copy number variation1nstd229human GRCh38 chr10: 115,336,016-115,342,733 , GRCh37.p13 chr10|NW_004775432.1: 309,480-316,197 , GRCh37.p13 chr10: 117,095,526-117,102,243 ATRNL1
    nsv6897976copy number variation1nstd229human GRCh38 chr10: 115,714,069-115,714,818 , GRCh37.p13 chr10|NW_004775432.1: 687,533-688,282 , GRCh37.p13 chr10: 117,473,579-117,474,328 ATRNL1
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