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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
    nsv4729071copy number variation1nstd102humanPathogenic GRCh37 chr8: 108,421,573-123,429,638 , GRCh38.p12 chr8: 107,409,345-122,417,399 RN7SL396P, LOC107986970, 124 more genes
    nsv4675222copy number variation1nstd102humanPathogenic GRCh37 chr8: 111,514,791-123,192,373 , GRCh38.p12 chr8: 110,502,562-122,180,134 LOC105375723, CSMD3, 93 more genes
    nsv4617341copy number variation1nstd183human GRCh37 chr8: 117,883,061-117,888,499 , GRCh38.p12 chr8: 116,870,822-116,876,260 RAD21-AS1, MIR3610, 1 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
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4168034copy number variation1nstd166human GRCh37.p13 chr8: 117,886,617-117,886,691 , GRCh38.p12 chr8: 116,874,378-116,874,452 RAD21-AS1, RAD21, 1 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
    nsv3923274copy number variation1nstd102humanUncertain significance NCBI36 chr8: 117,579,149-118,460,587 , GRCh38 chr8: 116,497,730-117,379,167 , GRCh37 chr8: 117,509,968-118,391,406 RN7SL826P, MIR3610, 14 more genes
    nsv3923146copy number variation1nstd102humanPathogenic GRCh38 chr8: 114,560,780-122,594,102 , NCBI36 chr8: 115,642,185-123,675,522 , GRCh37 chr8: 115,573,009-123,606,341 LOC105375721, LOC107986970, 73 more genes
    nsv3920738copy number variation1nstd102humanPathogenic GRCh38 chr8: 113,580,402-145,054,634 , NCBI36 chr8: 114,661,807-146,250,824 , GRCh37 chr8: 114,592,631-146,280,020 KHDRBS3, DENND3-AS1, 438 more genes
    nsv3920453copy number variation1nstd102humanPathogenic GRCh38 chr8: 113,418,060-120,975,305 , GRCh37 chr8: 114,430,289-121,987,545 , NCBI36 chr8: 114,499,465-122,056,726 LOC102723447, LOC105375721, 67 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
    nsv3919636copy number variation1nstd102humanPathogenic NCBI36 chr8: 101,948,747-146,266,575 , GRCh38 chr8: 100,867,343-145,070,385 , GRCh37 chr8: 101,879,571-146,295,771 RSPO2, MTND2P35, 592 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
    nsv3917391copy number variation1nstd102humanPathogenic NCBI36 chr8: 115,014,710-123,703,161 , GRCh37 chr8: 114,945,534-123,633,980 , GRCh38 chr8: 113,933,305-122,621,741 LOC107986968, DSCC1, 75 more genes
    nsv3916978copy number variation1nstd102humanPathogenic GRCh38 chr8: 86,300,584-137,022,587 , NCBI36 chr8: 87,381,929-138,104,012 , GRCh37 chr8: 87,312,813-138,034,830 MIR5194, TRS-AGA2-5, 601 more genes
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