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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6320462copy number variation1nstd223human GRCh38 chr1: 156,711,510-156,720,476 , GRCh37.p13 chr1: 156,681,302-156,690,268 ISG20L2
    nsv4784351copy number variation1nstd200human GRCh37 chr1: 156,687,985-156,690,160 , GRCh38.p12 chr1: 156,718,193-156,720,368 ISG20L2
    nsv4784352copy number variation1nstd200human GRCh37 chr1: 156,689,212-156,690,353 , GRCh38.p12 chr1: 156,719,420-156,720,561 ISG20L2
    nsv4897603copy number variation1nstd200human GRCh38 chr1: 156,719,454-156,720,548 , GRCh37.p13 chr1: 156,689,246-156,690,340 ISG20L2
    nsv3320236copy number variation1nstd162human GRCh38 chr1: 156,725,985-156,726,085 , GRCh37.p13 chr1: 156,695,777-156,695,877 ISG20L2
    nsv1174552copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr1: 156,682,786-156,690,796 , GRCh38.p12 chr1: 156,712,994-156,721,004 ISG20L2
    nsv5680670mobile element insertion1nstd211human GRCh38 chr1: 156,720,791-156,720,791 , GRCh37.p13 chr1: 156,690,583-156,690,583 ISG20L2
    esv2854292insertion1estd209human GRCh37 chr1: 156,692,055-156,692,055 , GRCh38.p12 chr1: 156,722,263-156,722,263 ISG20L2
    esv2854281insertion1estd209human GRCh37 chr1: 156,690,566-156,690,566 , GRCh38.p12 chr1: 156,720,774-156,720,774 ISG20L2
    esv1917062insertion1estd194human NCBI36 chr1: 154,957,191-154,957,191 , GRCh37.p13 chr1: 156,690,567-156,690,567 , GRCh38.p12 chr1: 156,720,775-156,720,775 ISG20L2
    nsv3088insertion1nstd2human NCBI35 chr1: 153,493,697-153,504,125 , GRCh37.p13 chr1: 156,680,624-156,691,052 , GRCh38.p12 chr1: 156,710,832-156,721,260 ISG20L2
    esv1202841insertion1estd22human NCBI36 chr1: 154,957,190-154,957,190 , GRCh37.p13 chr1: 156,690,566-156,690,566 , GRCh38.p12 chr1: 156,720,774-156,720,774 ISG20L2
    nsv1502437short tandem repeat6nstd128human GRCh37 chr1: 156,690,117-156,690,133 , GRCh38.p12 chr1: 156,720,325-156,720,341 ISG20L2
    nsv1465542short tandem repeat6nstd128human GRCh37 chr1: 156,692,398-156,692,412 , GRCh38.p12 chr1: 156,722,606-156,722,620 ISG20L2
    nsv1464164short tandem repeat4nstd128human GRCh37 chr1: 156,692,056-156,692,070 , GRCh38.p12 chr1: 156,722,264-156,722,278 ISG20L2
    nsv1464165short tandem repeat3nstd128human GRCh37 chr1: 156,694,750-156,694,761 , GRCh38.p12 chr1: 156,724,958-156,724,969 ISG20L2
    esv3352190copy number variation1estd59human NCBI36 chr1: 154,964,102-154,966,150 , GRCh37.p13 chr1: 156,697,478-156,699,526 , GRCh38.p12 chr1: 156,727,686-156,729,734 ISG20L2, METTL25B
    nsv6642772copy number variation1nstd229human GRCh38 chr1: 156,702,427-156,747,249 , GRCh37.p13 chr1: 156,672,219-156,717,041 ISG20L2, METTL25B, 3 more genes
    nsv4061286copy number variation1nstd166human GRCh37.p13 chr1: 156,672,219-156,717,044 , GRCh38.p12 chr1: 156,702,427-156,747,252 ISG20L2, METTL25B, 3 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 ISG20L2, CRB1, 1608 more genes
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