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Items: 1 to 20 of 506

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906686copy number variation1nstd209human GRCh38 chr2: 241,201,195-241,201,278 , GRCh37.p13 chr2: 242,140,610-242,140,693 ANO7
    nsv5905691copy number variation1nstd209human GRCh38 chr2: 241,210,775-241,210,899 , GRCh37.p13 chr2: 242,150,190-242,150,314 ANO7
    nsv5905552copy number variation1nstd209human GRCh38 chr2: 241,225,222-241,225,538 , GRCh37.p13 chr2: 242,164,637-242,164,953 HDLBP, ANO7, 1 more genes
    nsv5904998copy number variation1nstd209human GRCh38 chr2: 241,211,520-241,223,076 , GRCh37.p13 chr2: 242,150,935-242,162,491 ANO7
    nsv5903286copy number variation1nstd209human GRCh38 chr2: 241,205,288-241,205,345 , GRCh37.p13 chr2: 242,144,703-242,144,760 ANO7
    nsv5901471copy number variation1nstd209human GRCh38 chr2: 241,209,143-241,211,328 , GRCh37.p13 chr2: 242,148,558-242,150,743 ANO7
    nsv5833133copy number variation2nstd209human GRCh38 chr2: 241,209,842-241,210,841 , GRCh37.p13 chr2: 242,149,257-242,150,256 ANO7
    nsv5832832copy number variation1nstd209human GRCh38 chr2: 241,218,812-241,220,111 , GRCh37.p13 chr2: 242,158,227-242,159,526 ANO7
    nsv5832268copy number variation1nstd209human GRCh38 chr2: 241,209,142-241,217,060 , GRCh37.p13 chr2: 242,148,557-242,156,475 ANO7
    nsv5624490insertion1nstd207human GRCh38 chr2: 241,187,727-241,187,727 , GRCh37.p13 chr2: 242,127,142-242,127,142 LOC105373971, ANO7
    nsv5618502insertion1nstd207human GRCh38 chr2: 241,206,299-241,206,299 , GRCh37.p13 chr2: 242,145,714-242,145,714 ANO7
    nsv5618366insertion1nstd207human GRCh38 chr2: 241,187,779-241,187,779 , GRCh37.p13 chr2: 242,127,194-242,127,194 LOC105373971, ANO7
    nsv5617726insertion1nstd207human GRCh38 chr2: 241,218,158-241,218,158 , GRCh37.p13 chr2: 242,157,573-242,157,573 ANO7
    nsv5615611insertion1nstd207human GRCh38 chr2: 241,213,119-241,213,119 , GRCh37.p13 chr2: 242,152,534-242,152,534 ANO7
    nsv5615143insertion1nstd207human GRCh38 chr2: 241,207,064-241,207,064 , GRCh37.p13 chr2: 242,146,479-242,146,479 ANO7
    nsv5614435insertion1nstd207human GRCh38 chr2: 241,218,060-241,218,060 , GRCh37.p13 chr2: 242,157,475-242,157,475 ANO7
    nsv5613497insertion1nstd207human GRCh38 chr2: 241,213,109-241,213,109 , GRCh37.p13 chr2: 242,152,524-242,152,524 ANO7
    nsv5583435copy number variation1nstd207human GRCh38 chr2: 241,210,775-241,210,899 , GRCh37.p13 chr2: 242,150,190-242,150,314 ANO7
    nsv5579726copy number variation1nstd207human GRCh38 chr2: 241,205,828-241,206,121 , GRCh37.p13 chr2: 242,145,243-242,145,536 ANO7
    nsv5578008copy number variation1nstd207human GRCh38 chr2: 241,206,243-241,206,588 , GRCh37.p13 chr2: 242,145,658-242,146,003 ANO7
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