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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898720copy number variation1nstd209human GRCh38 chr3: 138,159,773-138,161,872 , GRCh37.p13 chr3: 137,878,615-137,880,714 DBR1
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5834678copy number variation1nstd209human GRCh38 chr3: 138,151,275-138,159,810 , GRCh37.p13 chr3: 137,870,117-137,878,652 DBR1
    nsv5834625copy number variation2nstd209human GRCh38 chr3: 138,172,872-138,174,071 , GRCh37.p13 chr3: 137,891,714-137,892,913 DBR1
    nsv5834624copy number variation1nstd209human GRCh38 chr3: 138,156,875-138,159,810 , GRCh37.p13 chr3: 137,875,717-137,878,652 DBR1
    nsv5834330copy number variation1nstd209human GRCh38 chr3: 138,160,161-138,161,738 , GRCh37.p13 chr3: 137,879,003-137,880,580 DBR1
    nsv5557303sequence alteration1nstd206human GRCh38 chr3: 138,151,310-138,160,094 , GRCh37.p13 chr3: 137,870,152-137,878,936 DBR1
    nsv5453618copy number variation1nstd206human GRCh38 chr3: 138,130,649-138,217,748 , GRCh37.p13 chr3: 137,849,491-137,936,590 ARMC8, DBR1, 1 more genes
    nsv5443170copy number variation1nstd206human GRCh38 chr3: 138,160,227-138,160,289 , GRCh37.p13 chr3: 137,879,069-137,879,131 DBR1
    nsv5361939translocation1nstd200human GRCh38 chr3: 138,160,095-138,160,095 , GRCh38 chr3: 138,156,686-138,156,686 , GRCh37.p13 chr3: 137,875,528-137,875,528 , GRCh37.p13 chr3: 137,878,937-137,878,937 DBR1
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4928002copy number variation1nstd200human GRCh38 chr3: 138,158,719-138,161,664 , GRCh37.p13 chr3: 137,877,561-137,880,506 DBR1
    nsv4928001copy number variation1nstd200human GRCh38 chr3: 138,151,279-138,160,123 , GRCh37.p13 chr3: 137,870,121-137,878,965 DBR1
    nsv4914801copy number variation1nstd200human GRCh38 chr3: 137,119,474-138,598,709 , GRCh37.p13 chr3: 136,838,316-138,317,551 , ESYT3, 18 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4587410copy number variation1nstd183human GRCh37 chr3: 137,880,269-137,880,405 , GRCh38.p12 chr3: 138,161,427-138,161,563 DBR1
    nsv4584850copy number variation1nstd183human GRCh37 chr3: 137,880,766-137,886,299 , GRCh38.p12 chr3: 138,161,924-138,167,457 DBR1
    nsv4584849copy number variation1nstd183human GRCh37 chr3: 137,848,325-137,934,622 , GRCh38.p12 chr3: 138,129,483-138,215,780 ARMC8, A4GNT, 1 more genes
    nsv4469354mobile element insertion1nstd166human GRCh37.p13 chr3: 137,888,133-137,888,133 , GRCh38.p12 chr3: 138,169,291-138,169,291 DBR1
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