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Items: 1 to 20 of 582

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 more genes
    nsv5945178copy number variation1nstd209human GRCh38 chr18: 689,842-690,334 , GRCh37.p13 chr18: 689,842-690,334 ENOSF1
    nsv5942919copy number variation1nstd209human GRCh38 chr18: 712,349-712,456 , GRCh37.p13 chr18: 712,349-712,456 ENOSF1
    nsv5930270copy number variation1nstd209human GRCh38 chr18: 675,407-684,987 , GRCh37.p13 chr18: 675,407-684,987 ENOSF1
    nsv5929721copy number variation1nstd209human GRCh38 chr18: 681,605-690,655 , GRCh37.p13 chr18: 681,605-690,655 ENOSF1
    nsv5928880copy number variation1nstd209human GRCh38 chr18: 691,459-698,964 , GRCh37.p13 chr18: 691,459-698,964 ENOSF1
    nsv5880192copy number variation1nstd209human GRCh38 chr18: 681,159-686,514 , GRCh37.p13 chr18: 681,159-686,514 ENOSF1
    nsv5873994copy number variation1nstd209human GRCh38 chr18: 691,440-698,756 , GRCh37.p13 chr18: 691,440-698,756 ENOSF1
    nsv5869811copy number variation1nstd209human GRCh38 chr18: 675,455-685,089 , GRCh37.p13 chr18: 675,455-685,089 ENOSF1
    nsv5654785insertion2nstd207human GRCh38 chr18: 712,349-712,349 , GRCh37.p13 chr18: 712,349-712,349 ENOSF1
    nsv5527192copy number variation1nstd206human GRCh38 chr18: 689,842-690,339 , GRCh37.p13 chr18: 689,842-690,339 ENOSF1
    nsv5520679copy number variation1nstd206human GRCh38 chr18: 699,248-699,352 , GRCh37.p13 chr18: 699,248-699,352 ENOSF1
    nsv5520555copy number variation1nstd206human GRCh38 chr18: 559,000-844,000 , GRCh37.p13 chr18: 559,000-844,001 RNU1-109P, LOC105371952, 8 more genes
    nsv5515153copy number variation1nstd206human GRCh38 chr18: 681,608-690,656 , GRCh37.p13 chr18: 681,608-690,656 ENOSF1
    nsv5514109copy number variation1nstd206human GRCh38 chr18: 350,000-744,000 , GRCh37.p13 chr18: 350,000-744,000 LOC107985155, LINC01925, 9 more genes
    nsv5375054translocation1nstd200human GRCh38 chr18: 684,175-684,175 , GRCh38 chr18: 3,312,068-3,312,068 , GRCh37.p13 chr18: 684,175-684,175 , GRCh37.p13 chr18: 3,312,066-3,312,066 ENOSF1
    nsv5375053translocation1nstd200human GRCh38 chr18: 701,251-701,251 , GRCh38 chr18: 643,091-643,091 , GRCh37.p13 chr18: 643,091-643,091 , GRCh37.p13 chr18: 701,251-701,251 ENOSF1, CLUL1
    nsv5349782translocation1nstd200human GRCh38 chr18: 987,434-987,434 , GRCh38 chr18: 707,824-707,824 , GRCh37.p13 chr18: 707,824-707,824 , GRCh37.p13 chr18: 987,435-987,435 ENOSF1, LOC107985165
    nsv5349781translocation1nstd200human GRCh38 chr18: 690,339-690,339 , GRCh38 chr18: 689,842-689,842 , GRCh37.p13 chr18: 689,842-689,842 , GRCh37.p13 chr18: 690,339-690,339 ENOSF1
    nsv5344938translocation1nstd200human GRCh37 chr18: 643,091-643,091 , GRCh37 chr18: 701,251-701,251 , GRCh38.p12 chr18: 643,091-643,091 , GRCh38.p12 chr18: 701,251-701,251 ENOSF1, CLUL1
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