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Items: 1 to 20 of 125

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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
    nsv7068795inversion1nstd229human GRCh38 chr17: 4,882,859-5,367,549 , GRCh37.p13 chr17: 4,786,154-5,270,844 CAMTA2, LOC105371505, 27 more genes
    nsv6993661copy number variation1nstd229human GRCh38 chr17: 5,109,588-5,120,681 , GRCh37.p13 chr17: 5,012,883-5,023,976 ZNF232, USP6, 1 more genes
    nsv6986403copy number variation1nstd229human GRCh38 chr17: 5,082,501-5,119,000 , GRCh37.p13 chr17: 4,985,796-5,022,295 USP6, ZNF232, 2 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
    nsv6979998copy number variation1nstd229human GRCh38 chr17: 5,097,188-5,155,464 , GRCh37.p13 chr17: 5,000,483-5,058,759 USP6, ZNF232-AS1, 1 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
    nsv6637426copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,867,994-5,233,679 , GRCh38.p12 chr17: 4,964,699-5,330,384 KIF1C, MIR6864, 17 more genes
    nsv6624291copy number variation1nstd224human GRCh37 chr17: 5,008,957-5,019,668 , GRCh38.p12 chr17: 5,105,662-5,116,373 ZNF232, ZNF232-AS1, 1 more genes
    nsv6624289copy number variation1nstd224human GRCh37 chr17: 4,948,344-6,354,965 , GRCh38.p12 chr17: 5,045,049-6,451,645 C1QBP, NUP88, 32 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
    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
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