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Items: 1 to 20 of 1356

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112733copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735 LOC112267888, LOC105373454, 40 more genes
    nsv5961786insertion1nstd209human GRCh38 chr2: 15,026,487-15,026,487 , GRCh37.p13 chr2: 15,166,611-15,166,611 NBAS
    nsv5959755insertion1nstd209human GRCh38 chr2: 15,098,354-15,098,354 , GRCh37.p13 chr2: 15,238,478-15,238,478 NBAS
    nsv5953757insertion1nstd209human GRCh38 chr2: 15,023,629-15,023,629 , GRCh37.p13 chr2: 15,163,753-15,163,753 NBAS
    nsv5948749insertion1nstd209human GRCh38 chr2: 15,379,415-15,379,415 , GRCh37.p13 chr2: 15,519,539-15,519,539 NBAS
    nsv5947838insertion1nstd209human GRCh38 chr2: 15,144,046-15,144,046 , GRCh37.p13 chr2: 15,284,170-15,284,170 NBAS
    nsv5887400copy number variation1nstd209human GRCh38 chr2: 15,146,259-15,152,172 , GRCh37.p13 chr2: 15,286,383-15,292,296 NBAS
    nsv5887020copy number variation1nstd209human GRCh38 chr2: 15,481,512-15,481,610 , GRCh37.p13 chr2: 15,621,636-15,621,734 NBAS
    nsv5886332copy number variation1nstd209human GRCh38 chr2: 15,098,117-15,098,187 , GRCh37.p13 chr2: 15,238,241-15,238,311 NBAS
    nsv5884509copy number variation1nstd209human GRCh38 chr2: 15,541,810-15,542,009 , GRCh37.p13 chr2: 15,681,934-15,682,133 NBAS
    nsv5882851copy number variation1nstd209human GRCh38 chr2: 15,026,161-15,026,486 , GRCh37.p13 chr2: 15,166,285-15,166,610 NBAS
    nsv5881299copy number variation1nstd209human GRCh38 chr2: 15,219,860-15,219,937 , GRCh37.p13 chr2: 15,359,984-15,360,061 NBAS
    nsv5881053copy number variation1nstd209human GRCh38 chr2: 15,097,986-15,098,382 , GRCh37.p13 chr2: 15,238,110-15,238,506 NBAS
    nsv5879482copy number variation1nstd209human GRCh38 chr2: 15,540,082-15,544,800 , GRCh37.p13 chr2: 15,680,206-15,684,924 NBAS
    nsv5876913copy number variation1nstd209human GRCh38 chr2: 15,144,923-15,147,922 , GRCh37.p13 chr2: 15,285,047-15,288,046 NBAS
    nsv5875629copy number variation1nstd209human GRCh38 chr2: 15,428,915-15,429,019 , GRCh37.p13 chr2: 15,569,039-15,569,143 NBAS
    nsv5875548copy number variation1nstd209human GRCh38 chr2: 15,047,548-15,047,694 , GRCh37.p13 chr2: 15,187,672-15,187,818 NBAS
    nsv5873359copy number variation1nstd209human GRCh38 chr2: 15,239,351-15,239,691 , GRCh37.p13 chr2: 15,379,475-15,379,815 NBAS
    nsv5871815copy number variation1nstd209human GRCh38 chr2: 15,016,319-15,057,662 , GRCh37.p13 chr2: 15,156,443-15,197,786 NBAS
    nsv5868734copy number variation1nstd209human GRCh38 chr2: 15,236,368-15,246,996 , GRCh37.p13 chr2: 15,376,492-15,387,120 NBAS
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