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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901079copy number variation1nstd209human GRCh38 chr2: 236,239,435-236,239,513 , GRCh37.p13 chr2: 237,148,078-237,148,156 ASB18
    nsv5897198copy number variation1nstd209human GRCh38 chr2: 236,229,960-236,230,409 , GRCh37.p13 chr2: 237,138,603-237,139,052 ASB18
    nsv5892488copy number variation1nstd209human GRCh38 chr2: 236,237,781-236,237,876 , GRCh37.p13 chr2: 237,146,424-237,146,519 ASB18
    nsv5578077copy number variation1nstd207human GRCh38 chr2: 236,239,435-236,239,513 , GRCh37.p13 chr2: 237,148,078-237,148,156 ASB18
    nsv5570308copy number variation1nstd207human GRCh38 chr2: 236,204,636-236,204,786 , GRCh37.p13 chr2: 237,113,279-237,113,429 ASB18
    nsv5565942copy number variation1nstd207human GRCh38 chr2: 236,237,334-236,237,383 , GRCh37.p13 chr2: 237,145,977-237,146,026 ASB18
    nsv5366894translocation1nstd200human GRCh38 chr2: 236,237,429-236,237,429 , GRCh38 chrX: 154,390,564-154,390,564 , GRCh37.p13 chrX: 153,618,906-153,618,906 , GRCh37.p13 chrX|NW_003871103.3: 1,824,543-1,824,543 , GRCh37.p13 chr2: 237,146,072-237,146,072 ASB18
    nsv5344704translocation1nstd200human GRCh37 chr2: 237,122,403-237,122,403 , GRCh37 chr2: 239,869,156-239,869,156 , GRCh38.p12 chr2: 238,947,460-238,947,460 , GRCh38.p12 chr2: 236,213,760-236,213,760 ASB18
    nsv5329121translocation1nstd204human GRCh38.p13 chr2: 238,947,460-238,947,460 , GRCh38.p13 chr2: 236,213,760-236,213,760 , GRCh37.p13 chr2: 237,122,403-237,122,403 , GRCh37.p13 chr2: 239,869,156-239,869,156 ASB18
    nsv5318856copy number variation1nstd204human GRCh38.p13 chr2: 236,094,899-237,206,460 , GRCh37.p13 chr2: 237,003,543-238,115,103 , LOC105373948, 20 more genes
    nsv5218666copy number variation1nstd204human GRCh38.p13 chr2: 235,186,401-236,356,900 , GRCh37.p13 chr2: 236,095,045-237,265,543 , AGAP1, 15 more genes
    nsv5217646copy number variation1nstd204human GRCh38.p13 chr2: 236,250,930-236,280,153 , GRCh37.p13 chr2: 237,159,573-237,188,796 ASB18
    nsv5213239copy number variation1nstd204human GRCh38.p13 chr2: 236,235,955-236,237,054 , GRCh37.p13 chr2: 237,144,598-237,145,697 ASB18
    nsv5212646copy number variation1nstd204human GRCh38.p13 chr2: 236,209,509-236,213,808 , GRCh37.p13 chr2: 237,118,152-237,122,451 ASB18, RNU1-31P
    nsv5210651copy number variation1nstd204human GRCh38.p13 chr2: 236,197,351-236,223,949 , GRCh37.p13 chr2: 237,105,994-237,132,592 RNU1-31P, ASB18
    nsv5077725mobile element insertion1nstd203human GRCh38 chr2: 236,230,551-236,230,561 , GRCh37.p13 chr2: 237,139,194-237,139,204 ASB18
    nsv5076854mobile element insertion1nstd203human GRCh38 chr2: 236,230,154-236,230,160 , GRCh37.p13 chr2: 237,138,797-237,138,803 ASB18
    nsv4926876copy number variation1nstd200human GRCh38 chr2: 236,252,521-236,253,883 , GRCh37.p13 chr2: 237,161,164-237,162,526 ASB18
    nsv4926875copy number variation1nstd200human GRCh38 chr2: 236,236,122-236,239,864 , GRCh37.p13 chr2: 237,144,765-237,148,507 ASB18
    nsv4926874copy number variation1nstd200human GRCh38 chr2: 236,222,868-236,227,182 , GRCh37.p13 chr2: 237,131,511-237,135,825 ASB18
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