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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv6992799copy number variation1nstd229human GRCh38 chr17: 4,703,601-4,840,000 , GRCh37.p13 chr17: 4,606,896-4,743,295 RPS12P29, PELP1-DT, 11 more genes
    nsv6982770copy number variation1nstd229human GRCh38 chr17: 3,468,201-5,384,400 , GRCh37.p13 chr17: 3,371,495-5,287,720 SLC25A11, CAMKK1, 83 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6979592copy number variation1nstd229human GRCh38 chr17: 4,273,434-4,887,250 , GRCh37.p13 chr17: 4,176,729-4,790,545 PELP1-DT, RPS12P29, 28 more genes
    nsv6638055copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,658,216-5,266,343 , GRCh38.p12 chr17: 4,754,921-5,363,048 RABEP1, SLC25A11, 33 more genes
    nsv6624288copy number variation1nstd224human GRCh37 chr17: 4,474,751-4,725,984 , GRCh38.p12 chr17: 4,571,456-4,822,689 TM4SF5, CXCL16, 17 more genes
    nsv6592364inversion1nstd223human GRCh38 chr17: 2,078,667-6,081,513 , GRCh37.p13 chr17: 1,981,961-5,984,833 MYBBP1A, CXCL16, 143 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6581467inversion1nstd223human GRCh38 chr17: 4,784,053-4,784,559 , GRCh37.p13 chr17: 4,687,348-4,687,854 VMO1
    nsv6505175copy number variation1nstd223human GRCh38 chr17: 4,772,769-4,787,562 , GRCh37.p13 chr17: 4,676,064-4,690,857 GLTPD2, VMO1, 1 more genes
    nsv6314802copy number variation1nstd102humanUncertain significance GRCh38 chr17: 4,772,213-5,119,909 , GRCh37.p13 chr17: 4,675,508-5,023,204 PFN1, ZNF232, 28 more genes
    nsv6314134copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,113,551-5,023,913 , GRCh38.p12 chr17: 4,210,256-5,120,618 ZNF232-AS1, RN7SL774P, 52 more genes
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 more genes
    nsv6133065copy number variation1nstd213human GRCh37 chr17: 4,530,000-8,270,001 , GRCh38.p12 chr17: 4,626,705-8,366,683 ACADVL, ALOX12, 206 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv5878783copy number variation1nstd209human GRCh38 chr17: 4,775,181-4,790,868 , GRCh37.p13 chr17: 4,678,476-4,694,163 GLTPD2, TM4SF5, 1 more genes
    nsv5299082copy number variation1nstd204human GRCh37.p13 chr17: 4,627,696-4,727,995 , GRCh38.p13 chr17: 4,724,401-4,824,700 PLD2, PSMB6, 6 more genes
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