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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095431copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,963,480-21,534,612 , GRCh38.p12 chr18: 21,383,519-23,954,648 MIB1, RN7SL233P, 41 more genes
    nsv7095001copy number variation1nstd102humanUncertain significance GRCh37 chr18: 19,383,858-19,780,786 , GRCh38.p12 chr18: 21,803,897-22,200,823 MIR1-2, LINC01900, 12 more genes
    nsv7001349copy number variation1nstd229human GRCh38 chr18: 21,822,053-21,827,015 , GRCh37.p13 chr18: 19,402,014-19,406,976 MIR133A1HG, MIR133A1, 2 more genes
    nsv6522145copy number variation1nstd223human GRCh38 chr18: 21,823,701-21,825,300 , GRCh37.p13 chr18: 19,403,662-19,405,261 MIB1, MIR133A1, 1 more genes
    nsv6517191copy number variation1nstd223human GRCh38 chr18: 21,822,053-21,827,015 , GRCh37.p13 chr18: 19,402,014-19,406,976 MIR133A1, MIB1, 2 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
    nsv6291540copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,611,942-26,843,691 , GRCh38.p12 chr18: 21,031,981-29,263,726 MIR133A1HG, LOC105372040, 111 more genes
    nsv6133378copy number variation1nstd213human GRCh37 chr18: 19,400,000-19,670,001 , GRCh38.p12 chr18: 21,820,039-22,090,040 RNA5SP451, MIR133A1HG, 8 more genes
    nsv5937759copy number variation1nstd209human GRCh38 chr18: 21,822,053-21,827,014 , GRCh37.p13 chr18: 19,402,014-19,406,975 MIR133A1, MIR1-2, 2 more genes
    nsv5872367copy number variation1nstd209human GRCh38 chr18: 21,822,078-21,826,789 , GRCh37.p13 chr18: 19,402,039-19,406,750 MIR133A1HG, MIB1, 1 more genes
    nsv5709873mobile element insertion1nstd211human GRCh38 chr18: 21,825,158-21,825,158 , GRCh37.p13 chr18: 19,405,119-19,405,119 MIB1, MIR133A1, 1 more genes
    nsv5422242mobile element insertion1nstd206human GRCh38 chr18: 21,825,158-21,825,209 , GRCh37.p13 chr18: 19,405,119-19,405,170 MIB1, MIR133A1, 1 more genes
    nsv5026866copy number variation1nstd200human GRCh38 chr18: 21,653,980-21,877,770 , GRCh37.p13 chr18: 19,233,941-19,457,731 , MIB1, 7 more genes
    nsv4854580copy number variation1nstd200human GRCh37 chr18: 19,402,014-19,406,976 , GRCh38.p12 chr18: 21,822,053-21,827,015 MIB1, MIR133A1, 2 more genes
    nsv4630265copy number variation1nstd183human GRCh37 chr18: 19,339,825-19,481,950 , GRCh38.p12 chr18: 21,759,864-21,901,989 MIB1, MIR1-2, 6 more genes
    nsv4561189mobile element insertion1nstd166human GRCh37.p13 chr18: 19,404,875-19,404,875 , GRCh38.p12 chr18: 21,824,914-21,824,914 MIB1, MIR133A1, 1 more genes
    nsv4457415copy number variation1nstd102humanUncertain significance GRCh37 chr18: 19,047,402-19,737,070 , GRCh38.p12 chr18: 21,467,441-22,157,109 ABHD3, RPL34P32, 15 more genes
    nsv4271360copy number variation1nstd166human GRCh37.p13 chr18: 19,402,028-19,406,976 , GRCh38.p12 chr18: 21,822,067-21,827,015 MIR133A1HG, MIR1-2, 2 more genes
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