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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965515copy number variation1nstd200human GRCh38 chr8: 79,766,523-80,173,455 , GRCh37.p13 chr8: 80,678,758-81,085,690 TPD52, LINC01607, 6 more genes
    nsv4829118copy number variation1nstd200human GRCh37 chr8: 80,678,758-81,085,690 , GRCh38.p12 chr8: 79,766,523-80,173,455 HEY1, LOC105375918, 6 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv3923698copy number variation1nstd102humanPathogenic NCBI36 chr8: 79,617,219-84,706,949 , GRCh37.p13 chr8: 79,454,664-84,544,394 , GRCh38.p12 chr8: 78,542,429-83,632,159 RPS26P34, PAG1, 77 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 more genes
    nsv3922848copy number variation1nstd102humanPathogenic NCBI36 chr8: 74,954,174-86,710,947 , GRCh37 chr8: 74,791,620-86,523,695 , GRCh38 chr8: 73,879,385-85,611,466 MITA1, CA3-AS1, 139 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3919841copy number variation1nstd102humanPathogenic GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824 LY6S-AS1, LOC107984017, 911 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3918656copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,817,543-82,252,186 , NCBI36 chr8: 75,980,098-82,414,741 , GRCh38 chr8: 74,905,308-81,339,951 ZFHX4, LOC105375916, 71 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 more genes
    nsv3916438copy number variation1nstd102humanPathogenic GRCh37 chr8: 46,942,962-140,297,737 , NCBI36 chr8: 47,062,127-140,366,919 , GRCh38 chr8: 46,031,340-139,285,494 NDUFS5P6, LINC01289, 1152 more genes
    nsv3916366copy number variation1nstd102humanPathogenic NCBI36 chr8: 78,554,841-146,264,902 , GRCh37 chr8: 78,392,286-146,294,098 , GRCh38 chr8: 77,480,050-145,068,712 FABP9, LOC101927040, 914 more genes
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