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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941062copy number variation1nstd209human GRCh38 chr17: 63,864,271-63,902,632 , GRCh37.p13 chr17: 61,941,631-61,979,992 , CSH1, 3 more genes
    nsv5885980copy number variation1nstd209human GRCh38 chr17: 63,867,869-63,878,677 , GRCh37.p13 chr17: 61,945,229-61,956,037 GH2, CSH2
    nsv5884690copy number variation1nstd209human GRCh38 chr17: 63,869,876-63,885,903 , GRCh37.p13 chr17: 61,947,236-61,963,263 , GH2, 1 more genes
    nsv5597748copy number variation1nstd207human GRCh38 chr17: 63,875,330-63,912,692 , GRCh37.p13 chr17: 61,952,690-61,990,052 , CSH1, 3 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5529934copy number variation1nstd206human GRCh38 chr17: 63,876,118-63,883,870 , GRCh37.p13 chr17: 61,953,478-61,961,230 , GH2
    nsv5527447copy number variation1nstd206human GRCh38 chr17: 63,875,698-63,898,250 , GRCh37.p13 chr17: 61,953,058-61,975,610 , CSH1, 1 more genes
    nsv5524798copy number variation1nstd206human GRCh38 chr17: 63,871,000-63,895,980 , GRCh37.p13 chr17: 61,948,360-61,973,340 , CSH2, 2 more genes
    nsv5329510copy number variation1nstd204human GRCh38.p13 chr17: 63,870,085-63,908,312 , GRCh37.p13 chr17: 61,947,445-61,985,672 , CSH2, 3 more genes
    nsv5300213copy number variation1nstd204human GRCh38.p13 chr17: 63,869,476-63,885,903 , GRCh37.p13 chr17: 61,946,836-61,963,263 , CSH2, 1 more genes
    nsv5300187copy number variation1nstd204human GRCh38.p13 chr17: 63,870,801-63,907,800 , GRCh37.p13 chr17: 61,948,161-61,985,160 , CSH1, 3 more genes
    nsv5297368copy number variation1nstd204human GRCh38.p13 chr17: 63,869,901-63,907,700 , GRCh37.p13 chr17: 61,947,261-61,985,060 , CSH1, 3 more genes
    nsv5295473copy number variation1nstd204human GRCh38.p13 chr17: 63,863,201-63,885,900 , GRCh37.p13 chr17: 61,940,561-61,963,260 , TCAM1P, 2 more genes
    nsv5293628copy number variation1nstd204human GRCh38.p13 chr17: 63,857,413-63,885,556 , GRCh37.p13 chr17: 61,934,773-61,962,916 , GH2, 2 more genes
    nsv5290744copy number variation1nstd204human GRCh38.p13 chr17: 63,869,776-63,882,302 , GRCh37.p13 chr17: 61,947,136-61,959,662 CSH2, GH2
    nsv5290430copy number variation1nstd204human GRCh38.p13 chr17: 63,881,176-63,883,038 , GRCh37.p13 chr17: 61,958,536-61,960,398 GH2
    nsv5288267copy number variation1nstd204human GRCh38.p13 chr17: 63,869,901-63,906,500 , GRCh37.p13 chr17: 61,947,261-61,983,860 , GH2, 2 more genes
    nsv5287320copy number variation1nstd204human GRCh38.p13 chr17: 63,881,903-63,884,440 , GRCh37.p13 chr17: 61,959,263-61,961,800 , GH2
    nsv5285161copy number variation1nstd204human GRCh38.p13 chr17: 63,867,394-63,908,101 , GRCh37.p13 chr17: 61,944,754-61,985,461 , CSHL1, 3 more genes
    nsv5285021copy number variation1nstd204human GRCh38.p13 chr17: 63,877,189-63,879,193 , GRCh37.p13 chr17: 61,954,549-61,956,553 GH2
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