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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
    nsv7094411copy number variation1nstd102humanPathogenic GRCh37 chr13: 52,531,632-52,532,700 , GRCh38.p12 chr13: 51,957,496-51,958,564 ATP7B
    nsv7094410copy number variation1nstd102humanUncertain significance GRCh37 chr13: 51,484,213-52,602,726 , GRCh38.p12 chr13: 50,910,077-52,028,590 ATP7B, RNA5SP29, 29 more genes
    nsv7094319copy number variation1nstd102humanPathogenic GRCh37 chr13: 52,548,990-52,552,030 , GRCh38.p12 chr13: 51,974,854-51,977,894 ATP7B
    nsv7094318copy number variation1nstd102humanPathogenic GRCh37 chr13: 52,516,512-52,516,700 , GRCh38.p12 chr13: 51,942,376-51,942,564 ATP7B
    nsv7094084copy number variation1nstd102humanPathogenic GRCh37 chr13: 52,508,892-52,585,473 , GRCh38.p12 chr13: 51,934,756-52,011,337 FABP5P2, ALG11, 1 more genes
    nsv7094004copy number variation1nstd102humanPathogenic GRCh37 chr13: 52,511,432-52,514,936 , GRCh38.p12 chr13: 51,937,296-51,940,800 ATP7B
    nsv7093334copy number variation1nstd102humanPathogenic GRCh38 chr13: 51,965,991-51,974,784 , GRCh37 chr13: 52,540,127-52,548,920 ATP7B, FABP5P2
    nsv7059629inversion1nstd229human GRCh38 chr13: 51,980,605-51,980,622 , GRCh37.p13 chr13: 52,554,741-52,554,758 ATP7B
    nsv6957279copy number variation1nstd229human GRCh38 chr13: 51,945,244-51,945,391 , GRCh37.p13 chr13: 52,519,380-52,519,527 ATP7B
    nsv6955933copy number variation1nstd229human GRCh38 chr13: 51,936,045-52,031,550 , GRCh37.p13 chr13: 52,510,181-52,605,686 UTP14C, ALG11, 2 more genes
    nsv6953997copy number variation1nstd229human GRCh38 chr13: 52,004,352-52,126,041 , GRCh37.p13 chr13: 52,578,488-52,700,177 ATP7B, NEK5, 2 more genes
    nsv6952539copy number variation1nstd229human GRCh38 chr13: 51,892,188-51,950,417 , GRCh37.p13 chr13: 52,466,324-52,524,553 ATP7B, CTAGE3P
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6951676copy number variation1nstd229human GRCh38 chr13: 51,999,001-52,025,200 , GRCh37.p13 chr13: 52,573,137-52,599,336 UTP14C, ATP7B, 1 more genes
    nsv6950466copy number variation1nstd229human GRCh38 chr13: 51,972,192-52,006,573 , GRCh37.p13 chr13: 52,546,328-52,580,709 ATP7B
    nsv6944138copy number variation1nstd229human GRCh38 chr13: 49,633,124-51,990,526 , GRCh37.p13 chr13: 50,207,260-52,564,662 LOC107984561, RPL5P31, 50 more genes
    nsv6944130copy number variation1nstd229human GRCh38 chr13: 51,979,042-51,979,429 , GRCh37.p13 chr13: 52,553,178-52,553,565 ATP7B
    nsv6941985copy number variation1nstd229human GRCh38 chr13: 51,745,017-52,075,317 , GRCh37.p13 chr13: 52,319,153-52,649,453 UTP14C, DHRS12, 9 more genes
    nsv6938835copy number variation1nstd229human GRCh38 chr13: 51,983,184-51,983,202 , GRCh37.p13 chr13: 52,557,320-52,557,338 ATP7B
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