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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5697921mobile element insertion1nstd211human GRCh38 chr17: 63,907,723-63,907,723 , GRCh37.p13 chr17: 61,985,083-61,985,083 CSHL1
    nsv5654251insertion1nstd207human GRCh38 chr17: 63,908,466-63,908,466 , GRCh37.p13 chr17: 61,985,826-61,985,826 CSHL1
    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
    nsv5533377copy number variation1nstd206human GRCh38 chr17: 63,906,475-64,023,565 , GRCh37.p13 chr17: 61,983,835-62,100,925 CD79B, CSHL1, 7 more genes
    nsv5515161copy number variation1nstd206human GRCh38 chr17: 63,893,862-63,908,550 , GRCh37.p13 chr17: 61,971,222-61,985,910 CSHL1, CSH1
    nsv5418948mobile element insertion1nstd206human GRCh38 chr17: 63,907,723-63,907,774 , GRCh37.p13 chr17: 61,985,083-61,985,134 CSHL1
    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
    nsv5300225copy number variation1nstd204human GRCh38.p13 chr17: 63,890,601-63,907,900 , GRCh37.p13 chr17: 61,967,961-61,985,260 CSH1, CSHL1
    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
    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
    nsv5282151copy number variation1nstd204human GRCh38.p13 chr17: 63,897,587-63,907,765 , GRCh37.p13 chr17: 61,974,947-61,985,125 CSHL1
    nsv5013920copy number variation1nstd200human GRCh38 chr17: 63,895,133-63,917,569 , GRCh37.p13 chr17: 61,972,493-61,994,929 CSH1, CSHL1, 2 more genes
    nsv5013919copy number variation1nstd200human GRCh38 chr17: 63,893,920-63,908,842 , GRCh37.p13 chr17: 61,971,280-61,986,202 CSHL1, CSH1
    nsv5013917copy number variation1nstd200human GRCh38 chr17: 63,881,722-63,911,272 , GRCh37.p13 chr17: 61,959,082-61,988,632 , CSH1, 3 more genes
    nsv5013916copy number variation1nstd200human GRCh38 chr17: 63,878,856-63,916,218 , GRCh37.p13 chr17: 61,956,216-61,993,578 , CSHL1, 4 more genes
    nsv5013915copy number variation1nstd200human GRCh38 chr17: 63,870,046-63,908,260 , GRCh37.p13 chr17: 61,947,406-61,985,620 , CSH1, 3 more genes
    nsv5010589copy number variation1nstd200human GRCh38 chr17: 63,897,616-63,912,267 , GRCh37.p13 chr17: 61,974,976-61,989,627 CSHL1, LOC112268204
    nsv5010583copy number variation1nstd200human GRCh38 chr17: 63,879,465-63,916,448 , GRCh37.p13 chr17: 61,956,825-61,993,808 , CSH1, 4 more genes
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