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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4680559copy number variation1nstd189human GRCh37.p13 chr8: 128,728,172-129,057,299 , GRCh38.p12 chr8: 127,715,926-128,045,053 MYC, PVT1, 7 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4674996copy number variation1nstd102humanPathogenic GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610 POU5F1B, DNAJC8P3, 158 more genes
    nsv4457220copy number variation1nstd102humanPathogenic GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646 ZHX1-C8orf76, SMILR, 117 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 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
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4455511copy number variation1nstd102humanPathogenic GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603 MTSS1, PCAT2, 148 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
    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
    nsv3921126copy number variation1nstd102humanPathogenic GRCh38 chr8: 122,454,392-128,513,076 , GRCh37 chr8: 123,466,631-129,525,322 , NCBI36 chr8: 123,535,812-129,594,504 DERL1, RNU6-442P, 101 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
    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
    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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