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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv6979306copy number variation1nstd229human GRCh38 chr17: 63,863,152-63,886,672 , GRCh37.p13 chr17: 61,940,512-61,964,032 CSH2, GH2, 1 more genes
    nsv6637179copy number variation1nstd102humanUncertain significance GRCh37 chr17: 61,838,634-62,465,444 , GRCh38.p12 chr17: 63,761,274-64,469,327 GH2, DDX42, 24 more genes
    nsv6624333copy number variation1nstd224human GRCh37 chr17: 61,947,107-61,978,548 , GRCh38.p12 chr17: 63,869,747-63,901,188 CSH1, CSH2, 1 more genes
    nsv6624104copy number variation16nstd224human GRCh37 chr17: 61,949,917-61,977,248 , GRCh38.p12 chr17: 63,872,557-63,899,888 CSH1, GH2, 1 more genes
    nsv6624098copy number variation1nstd224human GRCh37 chr17: 61,912,893-61,977,248 , GRCh38.p12 chr17: 63,835,533-63,899,888 CSH2, SMARCD2, 3 more genes
    nsv6531564copy number variation1nstd223human GRCh38 chr17: 63,871,301-63,885,900 , GRCh37.p13 chr17: 61,948,661-61,963,260 GH2, CSH2
    nsv6530743copy number variation1nstd223human GRCh38 chr17: 63,873,101-63,881,300 , GRCh37.p13 chr17: 61,950,461-61,958,660 GH2, CSH2
    nsv6529292copy number variation1nstd223human GRCh38 chr17: 63,870,401-63,872,800 , GRCh37.p13 chr17: 61,947,761-61,950,160 CSH2
    nsv6528262copy number variation1nstd223human GRCh38 chr17: 63,872,701-63,885,900 , GRCh37.p13 chr17: 61,950,061-61,963,260 GH2, CSH2
    nsv6526795copy number variation1nstd223human GRCh38 chr17: 63,863,444-63,901,765 , GRCh37.p13 chr17: 61,940,804-61,979,125 TCAM1P, CSH1, 2 more genes
    nsv6525565copy number variation1nstd223human GRCh38 chr17: 63,869,701-63,877,900 , GRCh37.p13 chr17: 61,947,061-61,955,260 CSH2
    nsv6524631copy number variation1nstd223human GRCh38 chr17: 63,870,001-63,907,700 , GRCh37.p13 chr17: 61,947,361-61,985,060 CSH2, CSHL1, 2 more genes
    nsv6524157copy number variation1nstd223human GRCh38 chr17: 63,872,301-63,895,200 , GRCh37.p13 chr17: 61,949,661-61,972,560 CSH1, CSH2, 1 more genes
    nsv6521272copy number variation1nstd223human GRCh38 chr17: 63,869,801-63,907,600 , GRCh37.p13 chr17: 61,947,161-61,984,960 GH2, CSH1, 1 more genes
    nsv6519873copy number variation1nstd223human GRCh38 chr17: 63,869,901-63,871,800 , GRCh37.p13 chr17: 61,947,261-61,949,160 CSH2
    nsv6519175copy number variation1nstd223human GRCh38 chr17: 63,866,369-63,889,280 , GRCh37.p13 chr17: 61,943,729-61,966,640 CSH2, GH2
    nsv6517090copy number variation1nstd223human GRCh38 chr17: 63,863,768-63,887,339 , GRCh37.p13 chr17: 61,941,128-61,964,699 CSH2, TCAM1P, 1 more genes
    nsv6516219copy number variation1nstd223human GRCh38 chr17: 63,873,618-63,918,780 , GRCh37.p13 chr17: 61,950,978-61,996,140 CSH1, CSH2, 4 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
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