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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098900copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,864,876-73,328,878 , GRCh38.p12 chr17: 74,868,753-75,332,797 CDR2L, OTOP2, 28 more genes
    nsv6997103copy number variation1nstd229human GRCh38 chr17: 75,136,964-75,139,521 , GRCh37.p13 chr17: 73,133,059-73,135,616 JPT1, LOC107985034
    nsv6993012copy number variation1nstd229human GRCh38 chr17: 75,136,251-75,147,554 , GRCh37.p13 chr17: 73,132,346-73,143,649 JPT1, LOC107985034
    nsv6985593copy number variation1nstd229human GRCh38 chr17: 75,140,036-75,144,590 , GRCh37.p13 chr17: 73,136,131-73,140,685 LOC107985034, JPT1
    nsv6985249copy number variation1nstd229human GRCh38 chr17: 75,137,940-75,146,490 , GRCh37.p13 chr17: 73,134,035-73,142,585 LOC107985034, JPT1
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6524264copy number variation1nstd223human GRCh38 chr17: 75,138,552-75,141,799 , GRCh37.p13 chr17: 73,134,647-73,137,894 JPT1, LOC107985034
    nsv6518255copy number variation1nstd223human GRCh38 chr17: 75,137,865-75,140,081 , GRCh37.p13 chr17: 73,133,960-73,136,176 JPT1, LOC107985034
    nsv6314018copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,049,227-73,533,226 , GRCh38.p12 chr17: 75,053,132-75,537,145 MIF4GD-DT, TSEN54, 21 more genes
    nsv6291659copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,045,938-73,310,951 , GRCh38.p12 chr17: 75,049,843-75,314,870 SLC25A19, NUP85, 12 more genes
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv6024147copy number variation1nstd212human GRCh38 chr17: 75,142,562-75,142,622 , GRCh37.p13 chr17: 73,138,657-73,138,717 LOC107985034, JPT1
    nsv5940138copy number variation1nstd209human GRCh38 chr17: 75,150,442-75,175,508 , GRCh37.p13 chr17: 73,146,537-73,171,603 JPT1, SUMO2
    nsv5875335copy number variation1nstd209human GRCh38 chr17: 75,151,488-75,160,298 , GRCh37.p13 chr17: 73,147,583-73,156,393 JPT1
    nsv5652523insertion1nstd207human GRCh38 chr17: 75,139,819-75,139,819 , GRCh37.p13 chr17: 73,135,914-73,135,914 JPT1, LOC107985034
    nsv5521559copy number variation1nstd206human GRCh38 chr17: 75,140,678-75,141,417 , GRCh37.p13 chr17: 73,136,773-73,137,512 JPT1, LOC107985034
    nsv5298973copy number variation1nstd204human GRCh38.p13 chr17: 74,951,501-75,212,200 , GRCh37.p13 chr17: 72,947,596-73,208,295 RNU6-362P, TRR-CCT2-1, 17 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
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