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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914088copy number variation1nstd209human GRCh38 chr8: 125,933,731-125,939,314 , GRCh37.p13 chr8: 126,945,975-126,951,558 LINC00861
    nsv5853457copy number variation1nstd209human GRCh38 chr8: 125,933,892-125,939,310 , GRCh37.p13 chr8: 126,946,136-126,951,554 LINC00861
    nsv5480238copy number variation1nstd206human GRCh38 chr8: 125,933,735-125,939,315 , GRCh37.p13 chr8: 126,945,979-126,951,559 LINC00861
    nsv5379413translocation1nstd200human GRCh38 chr8: 125,932,252-125,932,252 , GRCh38 chr8: 125,932,331-125,932,331 , GRCh37.p13 chr8: 126,944,575-126,944,575 , GRCh37.p13 chr8: 126,944,496-126,944,496 LINC00861
    nsv5116912mobile element insertion1nstd203human GRCh38 chr8: 125,936,001-125,936,015 , GRCh37.p13 chr8: 126,948,245-126,948,259 LINC00861
    nsv5114560mobile element insertion1nstd203human GRCh38 chr8: 125,948,859-125,948,888 , GRCh37.p13 chr8: 126,961,103-126,961,132 LINC00861
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4813426copy number variation1nstd200human GRCh37 chr8: 126,955,641-126,955,696 , GRCh38.p12 chr8: 125,943,397-125,943,452 LINC00861
    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
    nsv4482444mobile element insertion1nstd166human GRCh37.p13 chr8: 126,948,245-126,948,245 , GRCh38.p12 chr8: 125,936,001-125,936,001 LINC00861
    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
    nsv4412277copy number variation1nstd174human GRCh37 chr8: 126,945,937-126,955,037 , GRCh38.p12 chr8: 125,933,693-125,942,793 LINC00861
    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
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