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Items: 1 to 20 of 499

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 TAOK2, SLC7A5P1, 44 more genes
    nsv6112812copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,200,008 , GRCh38.p12 chr16: 29,663,729-30,188,687 INO80E, QPRT, 33 more genes
    nsv6112806copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,218,221 , GRCh38.p12 chr16: 29,663,729-30,206,900 YPEL3-DT, PAGR1, 38 more genes
    nsv6112788copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,615,859-30,199,454 , GRCh38.p12 chr16: 29,604,538-30,188,133 ALDOA, MVP, 36 more genes
    nsv5980454copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,545,794-30,307,472 , GRCh38.p12 chr16: 29,534,473-30,296,151 LOC105371167, MIR3680-2, 46 more genes
    nsv5938679copy number variation1nstd209human GRCh38 chr16: 29,576,286-30,317,646 , GRCh37.p13 chr16: 29,587,607-30,328,967 , BOLA2B, 47 more genes
    nsv5672756copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,044-30,212,202 , GRCh38.p12 chr16: 29,663,723-30,200,881 ALDOA, QPRT, 37 more genes
    nsv5564226copy number variation7nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 29,802,081-30,199,917 , GRCh38.p12 chr16: 29,790,760-30,188,596 MAPK3, MAZ, 27 more genes
    nsv5533861copy number variation1nstd206human GRCh38 chr16: 29,969,559-29,970,138 , GRCh37.p13 chr16: 29,980,880-29,981,459 TMEM219
    nsv5525049copy number variation1nstd206human GRCh38 chr16: 29,966,770-29,966,898 , GRCh37.p13 chr16: 29,978,091-29,978,219 TMEM219
    nsv5522140copy number variation1nstd206human GRCh38 chr16: 29,967,720-29,971,170 , GRCh37.p13 chr16: 29,979,041-29,982,491 TMEM219
    nsv5519942copy number variation1nstd206human GRCh38 chr16: 29,446,486-30,285,000 , GRCh37.p13 chr16: 29,457,807-30,296,321 , CA5AP1, 57 more genes
    nsv5517048copy number variation1nstd206human GRCh38 chr16: 29,962,027-29,962,106 , GRCh37.p13 chr16: 29,973,348-29,973,427 TMEM219
    nsv5516853copy number variation1nstd206human GRCh38 chr16: 29,966,614-29,967,802 , GRCh37.p13 chr16: 29,977,935-29,979,123 TMEM219
    nsv5380931copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 29,802,081-30,200,285 , GRCh38.p12 chr16: 29,790,760-30,188,964 CDIPTOSP, MAZ, 27 more genes
    nsv5302014copy number variation1nstd204human GRCh38.p13 chr16: 29,969,533-29,970,167 , GRCh37.p13 chr16: 29,980,854-29,981,488 TMEM219
    nsv5278770copy number variation1nstd204human GRCh38.p13 chr16: 29,940,116-29,984,520 , GRCh37.p13 chr16: 29,951,437-29,995,841 TMEM219, TAOK2
    nsv5274738copy number variation1nstd204human GRCh38.p13 chr16: 29,950,029-29,982,276 , GRCh37.p13 chr16: 29,961,350-29,993,597 TMEM219, TAOK2
    nsv5200388copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,652,999-30,198,600 , GRCh38.p12 chr16: 29,641,678-30,187,279 PAGR1, MVP, 33 more genes
    nsv5200382copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,673,954-30,198,600 , GRCh38.p12 chr16: 29,662,633-30,187,279 TMEM219, INO80E, 33 more genes
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