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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
    nsv6525565copy number variation1nstd223human GRCh38 chr17: 63,869,701-63,877,900 , GRCh37.p13 chr17: 61,947,061-61,955,260 CSH2
    nsv6529292copy number variation1nstd223human GRCh38 chr17: 63,870,401-63,872,800 , GRCh37.p13 chr17: 61,947,761-61,950,160 CSH2
    nsv6519873copy number variation1nstd223human GRCh38 chr17: 63,869,901-63,871,800 , GRCh37.p13 chr17: 61,947,261-61,949,160 CSH2
    nsv4260540copy number variation1nstd166human GRCh37.p13 chr17: 61,949,436-61,949,493 , GRCh38.p12 chr17: 63,872,076-63,872,133 CSH2
    nsv5287161copy number variation1nstd204human GRCh38.p13 chr17: 63,869,976-63,874,666 , GRCh37.p13 chr17: 61,947,336-61,952,026 CSH2
    nsv5282488copy number variation1nstd204human GRCh38.p13 chr17: 63,870,635-63,871,847 , GRCh37.p13 chr17: 61,947,995-61,949,207 CSH2
    nsv5880517copy number variation2nstd209human GRCh38 chr17: 63,871,548-63,873,235 , GRCh37.p13 chr17: 61,948,908-61,950,595 CSH2
    esv2427129insertion1estd197human NCBI36 chr17: 59,301,115-59,301,115 , GRCh37.p13 chr17: 61,947,383-61,947,383 , GRCh38.p12 chr17: 63,870,023-63,870,023 CSH2
    esv2380584insertion1estd194human NCBI36 chr17: 59,301,116-59,301,116 , GRCh37.p13 chr17: 61,947,384-61,947,384 , GRCh38.p12 chr17: 63,870,024-63,870,024 CSH2
    nsv6519175copy number variation1nstd223human GRCh38 chr17: 63,866,369-63,889,280 , GRCh37.p13 chr17: 61,943,729-61,966,640 CSH2, GH2
    nsv6530743copy number variation1nstd223human GRCh38 chr17: 63,873,101-63,881,300 , GRCh37.p13 chr17: 61,950,461-61,958,660 CSH2, GH2
    nsv6531564copy number variation1nstd223human GRCh38 chr17: 63,871,301-63,885,900 , GRCh37.p13 chr17: 61,948,661-61,963,260 CSH2, GH2
    nsv6528262copy number variation1nstd223human GRCh38 chr17: 63,872,701-63,885,900 , GRCh37.p13 chr17: 61,950,061-61,963,260 CSH2, GH2
    nsv5290744copy number variation1nstd204human GRCh38.p13 chr17: 63,869,776-63,882,302 , GRCh37.p13 chr17: 61,947,136-61,959,662 CSH2, GH2
    nsv5877190copy number variation1nstd209human GRCh38 chr17: 63,864,243-63,877,288 , GRCh37.p13 chr17: 61,941,603-61,954,648 CSH2, TCAM1P
    nsv5885980copy number variation1nstd209human GRCh38 chr17: 63,867,869-63,878,677 , GRCh37.p13 chr17: 61,945,229-61,956,037 CSH2, GH2
    nsv4264682copy number variation1nstd166human GRCh37.p13 chr17: 61,940,000-61,950,000 , GRCh38.p12 chr17: 63,862,640-63,872,640 CSH2, TCAM1P
    nsv3895088copy number variation1nstd102humanBenign GRCh37 chr17: 61,915,326-61,983,601 , GRCh38.p12 chr17: 63,837,966-63,906,241 CSH2, CSH1, 3 more genes
    nsv3891336copy number variation1nstd102humanLikely benign GRCh37 chr17: 61,940,902-61,986,943 , GRCh38.p12 chr17: 63,863,542-63,909,583 CSH2, CSH1, 3 more genes
    nsv3896655copy number variation1nstd102humanLikely benign GRCh37 chr17: 61,937,184-61,973,673 , GRCh38.p12 chr17: 63,859,824-63,896,313 CSH2, CSH1, 2 more genes
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