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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095411copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,534,311-63,537,685 , GRCh38.p12 chr17: 65,538,193-65,541,567 AXIN2
    nsv7095358copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,545,628-63,554,738 , GRCh38.p12 chr17: 65,549,510-65,558,620 AXIN2
    nsv7093125copy number variation1nstd102humanUncertain significance GRCh38 chr17: 65,533,815-65,533,906 , GRCh37 chr17: 63,529,933-63,530,024 AXIN2
    nsv7077537inversion1nstd229human GRCh38 chr17: 64,968,697-68,255,761 , GRCh37.p13 chr17: 62,964,815-65,936,105 SNORA38B, PRKCA-AS1, 52 more genes
    nsv7072812inversion1nstd229human GRCh38 chr17: 65,534,213-65,534,335 , GRCh37.p13 chr17: 63,530,331-63,530,453 AXIN2
    nsv7070779inversion1nstd229human GRCh38 chr17: 64,711,213-68,088,947 , GRCh37.p13 chr17: 62,707,331-65,936,105 MICOS10P2, LOC100420638, 61 more genes
    nsv7070446inversion1nstd229human GRCh38 chr17: 65,003,854-68,220,374 , GRCh37.p13 chr17: 62,999,972-65,936,105 SH3GL1P3, AXIN2, 51 more genes
    nsv7067455inversion1nstd229human GRCh38 chr17: 65,555,132-65,555,195 , GRCh37.p13 chr17: 63,551,250-63,551,313 AXIN2
    nsv7059173inversion1nstd229human GRCh38 chr17: 65,003,895-68,220,334 , GRCh37.p13 chr17: 63,000,013-65,936,105 RPSAP67, HELZ-AS1, 51 more genes
    nsv6995621copy number variation1nstd229human GRCh38 chr17: 65,538,094-65,538,135 , GRCh37.p13 chr17: 63,534,212-63,534,253 AXIN2
    nsv6992357copy number variation1nstd229human GRCh38 chr17: 65,549,813-65,551,616 , GRCh37.p13 chr17: 63,545,931-63,547,734 AXIN2
    nsv6991687copy number variation1nstd229human GRCh38 chr17: 65,555,019-65,555,216 , GRCh37.p13 chr17: 63,551,137-63,551,334 AXIN2
    nsv6990400copy number variation1nstd229human GRCh38 chr17: 65,549,101-65,564,800 , GRCh37.p13 chr17: 63,545,219-63,560,918 AXIN2
    nsv6988811copy number variation1nstd229human GRCh38 chr17: 65,493,421-65,572,586 , GRCh37.p13 chr17: 63,489,539-63,568,704 AXIN2
    nsv6980450copy number variation1nstd229human GRCh38 chr17: 65,520,099-65,541,468 , GRCh37.p13 chr17: 63,516,217-63,537,586 AXIN2
    nsv6310403copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,526,094-63,530,207 , GRCh38.p12 chr17: 65,529,976-65,534,089 AXIN2
    nsv6310402copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,526,094-63,526,230 , GRCh38.p12 chr17: 65,529,976-65,530,112 AXIN2
    nsv6310331copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,531,734-63,554,738 , GRCh38.p12 chr17: 65,535,616-65,558,620 AXIN2
    nsv6310187copy number variation1nstd102humanUncertain significance GRCh37 chr17: 63,529,041-63,531,806 , GRCh38.p12 chr17: 65,532,923-65,535,688 AXIN2
    nsv6259001mobile element insertion1nstd215human GRCh38 chr17: 65,553,859-65,553,859 , GRCh37.p13 chr17: 63,549,977-63,549,977 AXIN2
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