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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5828344copy number variation1nstd209human GRCh37.p13 chr1|NW_003871055.3: 6,653,503-6,665,656 , GRCh38 chr1: 149,838,090-149,850,243 , GRCh37.p13 chr1: 149,809,652-149,821,810 H2BC20P, H2BC19P, 3 more genes
    nsv5672211inversion1nstd207human GRCh38 chr1: 149,817,539-149,876,316 , GRCh37.p13 chr1: 149,789,093-149,847,866 , GRCh37.p13 chr1|NW_003871055.3: 6,632,952-6,691,729 H2AC18, H4C14, 6 more genes
    nsv5423100copy number variation1nstd206human GRCh37.p13 chr1|NW_003871055.3: 6,658,000-6,666,000 , GRCh38 chr1: 149,842,587-149,850,587 , GRCh37.p13 chr1: 149,814,154-149,822,154 H2AC18, H2AC19, 2 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5370546translocation1nstd200human GRCh38 chr1: 149,843,898-149,843,898 , GRCh38 chr1: 149,848,767-149,848,767 , GRCh37.p13 chr1: 149,815,465-149,815,465 , GRCh37.p13 chr1: 149,820,334-149,820,334 , GRCh37.p13 chr1|NW_003871055.3: 6,659,311-6,659,311 , GRCh37.p13 chr1|NW_003871055.3: 6,664,180-6,664,180 H2BC20P, H2BC19P
    nsv5209954copy number variation1nstd204human GRCh38.p13 chr1: 149,846,444-149,848,443 , GRCh37.p13 chr1: 149,818,011-149,820,010 , GRCh37.p13 chr1|NW_003871055.3: 6,661,857-6,663,856 H2BC20P
    nsv5208677copy number variation1nstd204human GRCh38.p13 chr1: 149,845,401-149,851,700 , GRCh37.p13 chr1|NW_003871055.3: 6,660,814-6,667,113 , GRCh37.p13 chr1: 149,816,968-149,823,262 H2BC20P, H3C15, 1 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4730064inversion26nstd198human GRCh38 chr1: 149,816,748-149,876,338 , GRCh37.p13 chr1: 149,788,302-149,847,888 , GRCh37.p13 chr1|NW_003871055.3: 6,632,161-6,691,751 H2AC18, H4C14, 6 more genes
    nsv4714233copy number variation1nstd195human GRCh37 chr1: 149,814,801-149,822,101 , GRCh38.p12 chr1: 149,843,234-149,850,534 H2AC18, H2BC20P, 2 more genes
    nsv4658003inversion1nstd185human GRCh37.p13 chr1|NW_003871055.3: 6,658,931-6,665,707 , GRCh37.p13 chr1: 149,815,085-149,821,861 , GRCh38.p13 chr1: 149,843,518-149,850,294 H2BC20P, H2BC19P, 1 more genes
    nsv4593941copy number variation1nstd183human GRCh37 chr1: 149,816,200-149,844,995 , GRCh38.p12 chr1: 149,844,633-149,873,445 H2BC20P, H4C15, 2 more genes
    nsv4579553copy number variation1nstd183human GRCh37 chr1: 149,791,739-149,872,081 , GRCh38.p12 chr1: 149,820,184-149,900,528 H2BC21, H4C15, 10 more genes
    nsv4579291copy number variation1nstd183human GRCh37 chr1: 149,788,216-149,857,110 , GRCh38.p12 chr1: 149,816,662-149,885,560 H3C15, H2AC19, 9 more genes
    nsv4579195copy number variation1nstd183human GRCh37 chr1: 149,815,145-149,821,869 , GRCh38.p12 chr1: 149,843,578-149,850,302 H2BC20P, H2BC19P, 1 more genes
    nsv4386636copy number variation1nstd173human GRCh37 chr1: 149,803,428-149,825,762 , GRCh38.p12 chr1: 149,831,864-149,854,200 H2AC18, H4C14, 5 more genes
    nsv4053532copy number variation1nstd166human GRCh37.p13 chr1: 149,814,850-149,821,650 , GRCh38.p12 chr1: 149,843,283-149,850,083 H2AC19, H2BC20P, 1 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 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 , CRB1, 1608 more genes
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