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Items: 1 to 20 of 635

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125067insertion1nstd186human GRCh37 chr2: 242,830,049-242,830,051 , GRCh38.p12 chr2: 241,887,898-241,887,900 , GRCh38.p12 chr2|NT_187527.1: 99,996-99,998 LINC01237
    nsv6124806insertion1nstd186human GRCh37 chr2: 242,901,083-242,901,116 , GRCh38.p12 chr2|NT_187527.1: 171,793-171,826 , GRCh38.p12 chr2: 241,958,932-241,958,965 LINC01237
    nsv5389110copy number variation1nstd186human GRCh37 chr2: 242,816,954-242,817,201 , GRCh38.p12 chr2|NT_187527.1: 86,901-87,148 , GRCh38.p12 chr2: 241,874,803-241,875,050 0
    nsv5388774copy number variation1nstd186human GRCh37 chr2: 242,760,572-242,762,352 , GRCh38.p12 chr2: 241,819,244-241,820,167 , GRCh38.p12 chr2|NT_187527.1: 31,371-32,267 LOC107986004
    nsv5388686copy number variation2nstd186human GRCh37 chr2: 242,753,582-242,753,825 , GRCh38.p12 chr2|NT_187527.1: 24,585-24,785 , GRCh38.p12 chr2: 241,812,487-241,812,687 NEU4
    nsv5388546copy number variation1nstd186human GRCh37 chr2: 242,816,954-242,817,202 , GRCh38.p12 chr2|NT_187527.1: 86,901-87,149 , GRCh38.p12 chr2: 241,874,803-241,875,051 0
    nsv5388403copy number variation1nstd186human GRCh37 chr2: 242,830,868-242,830,998 , GRCh38.p12 chr2: 241,888,717-241,888,847 , GRCh38.p12 chr2|NT_187527.1: 100,815-100,945 LINC01237
    nsv5387737copy number variation1nstd186human GRCh37 chr2: 242,830,626-242,830,869 , GRCh38.p12 chr2: 241,888,475-241,888,718 , GRCh38.p12 chr2|NT_187527.1: 100,573-100,816 LINC01237
    nsv5387182copy number variation1nstd186human GRCh37 chr2: 242,869,774-242,870,609 , GRCh38.p12 chr2|NT_187527.1: 139,762-140,596 , GRCh38.p12 chr2: 241,927,623-241,928,458 LINC01237
    nsv5385491copy number variation1nstd186human GRCh37 chr2: 242,869,779-242,870,605 , GRCh38.p12 chr2|NT_187527.1: 139,767-140,592 , GRCh38.p12 chr2: 241,927,628-241,928,454 LINC01237
    nsv5335312translocation1nstd200human GRCh37 chr2: 242,903,310-242,903,310 , GRCh37 chr2: 243,178,155-243,178,155 , GRCh38.p12 chr2: 241,961,159-241,961,159 , GRCh38.p12 chr2: 242,157,851-242,157,851 , GRCh38.p12 chr2|NT_187527.1: 174,020-174,020 LINC01237, LINC01881
    nsv5329875translocation1nstd200human GRCh37 chr2: 242,802,325-242,802,325 , GRCh37 chr2: 242,802,262-242,802,262 , GRCh38.p12 chr2: 241,860,173-241,860,173 , GRCh38.p12 chr2: 241,860,110-241,860,110 , GRCh38.p12 chr2|NT_187527.1: 72,271-72,271 , GRCh38.p12 chr2|NT_187527.1: 72,208-72,208 0
    nsv4804755copy number variation1nstd200human GRCh37 chr2: 242,869,622-242,870,942 , GRCh38.p12 chr2: 241,927,471-241,928,791 , GRCh38.p12 chr2|NT_187527.1: 139,610-140,929 LINC01237
    nsv4804754copy number variation1nstd200human GRCh37 chr2: 242,816,951-242,817,202 , GRCh38.p12 chr2|NT_187527.1: 86,898-87,149 , GRCh38.p12 chr2: 241,874,800-241,875,051 0
    nsv4804753copy number variation1nstd200human GRCh37 chr2: 242,753,582-242,753,825 , GRCh38.p12 chr2|NT_187527.1: 24,585-24,785 , GRCh38.p12 chr2: 241,812,487-241,812,687 NEU4
    nsv4790209copy number variation1nstd200human GRCh37 chr2: 242,873,415-242,874,664 , GRCh38.p12 chr2: 241,931,264-241,932,513 , GRCh38.p12 chr2|NT_187527.1: 144,135-145,384 LINC01237
    nsv4790208copy number variation1nstd200human GRCh37 chr2: 242,864,073-242,936,009 , GRCh38.p12 chr2|NT_187527.1: 134,099-174,166 , GRCh38.p12 chr2: 241,921,922-241,993,858 LINC01238, LINC01237
    nsv4790206copy number variation1nstd200human GRCh37 chr2: 242,853,118-242,857,774 , GRCh38.p12 chr2|NT_187527.1: 123,065-127,721 , GRCh38.p12 chr2: 241,910,967-241,915,623 LINC01237
    nsv4790205copy number variation1nstd200human GRCh37 chr2: 242,840,694-242,854,414 , GRCh38.p12 chr2: 241,898,543-241,912,263 , GRCh38.p12 chr2|NT_187527.1: 110,641-124,361 LINC01237, FAM240C
    nsv4790204copy number variation1nstd200human GRCh37 chr2: 242,830,618-242,830,872 , GRCh38.p12 chr2: 241,888,467-241,888,721 , GRCh38.p12 chr2|NT_187527.1: 100,565-100,819 LINC01237
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