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Items: 1 to 20 of 153

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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
    nsv7098689copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,801,983-4,802,032 , GRCh38 chr17: 4,898,688-4,898,737 CHRNE, C17orf107
    nsv7093604insertion1nstd102humanPathogenic GRCh37 chr17: 4,802,827-4,802,827 , GRCh38 chr17: 4,899,532-4,899,532 CHRNE, C17orf107
    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
    nsv6991124copy number variation1nstd229human GRCh38 chr17: 4,897,777-4,900,911 , GRCh37.p13 chr17: 4,801,072-4,804,206 C17orf107, MINK1, 1 more genes
    nsv6985628copy number variation1nstd229human GRCh38 chr17: 4,867,448-4,906,651 , GRCh37.p13 chr17: 4,770,743-4,809,946 CHRNE, MINK1, 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
    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
    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
    nsv6502799copy number variation1nstd223human GRCh38 chr17: 4,901,974-4,902,776 , GRCh37.p13 chr17: 4,805,269-4,806,071 CHRNE, C17orf107
    nsv6502092copy number variation1nstd223human GRCh38 chr17: 4,869,520-4,948,195 , GRCh37.p13 chr17: 4,772,815-4,851,490 MINK1, C17orf107, 7 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
    nsv6310179copy number variation1nstd102humanPathogenic GRCh37 chr17: 4,805,539-4,806,690 , GRCh38.p12 chr17: 4,902,244-4,903,395 C17orf107, CHRNE
    nsv6310178copy number variation1nstd102humanPathogenic GRCh37 chr17: 4,802,021-4,802,196 , GRCh38.p12 chr17: 4,898,726-4,898,901 CHRNE, C17orf107
    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
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