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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912925copy number variation1nstd209human GRCh38 chr11: 93,684,940-93,685,840 , GRCh37.p13 chr11: 93,418,106-93,419,006 CEP295
    nsv5697068mobile element insertion1nstd211human GRCh38 chr11: 93,677,306-93,677,306 , GRCh37.p13 chr11: 93,410,472-93,410,472 CEP295
    nsv5656511insertion1nstd207human GRCh38 chr11: 93,685,841-93,685,841 , GRCh37.p13 chr11: 93,419,007-93,419,007 CEP295
    nsv5501490copy number variation1nstd206human GRCh38 chr11: 93,684,940-93,685,841 , GRCh37.p13 chr11: 93,418,106-93,419,007 CEP295
    nsv5497804copy number variation1nstd206human GRCh38 chr11: 93,482,000-94,038,896 , GRCh37.p13 chr11: 93,215,166-93,772,062 SNORA1, HPRT1P3, 20 more genes
    nsv5495810copy number variation1nstd206human GRCh38 chr11: 93,692,194-93,692,885 , GRCh37.p13 chr11: 93,425,360-93,426,051 CEP295
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373802translocation1nstd200human GRCh38 chr11: 93,685,841-93,685,841 , GRCh38 chr11: 93,684,940-93,684,940 , GRCh37.p13 chr11: 93,418,106-93,418,106 , GRCh37.p13 chr11: 93,419,007-93,419,007 CEP295
    nsv5348130translocation1nstd200human GRCh38 chr11: 93,692,885-93,692,885 , GRCh38 chr11: 93,692,194-93,692,194 , GRCh37.p13 chr11: 93,425,360-93,425,360 , GRCh37.p13 chr11: 93,426,051-93,426,051 CEP295
    nsv5348128translocation1nstd200human GRCh38 chr11: 93,667,364-93,667,364 , GRCh38 chr11: 93,667,467-93,667,467 , GRCh37.p13 chr11: 93,400,530-93,400,530 , GRCh37.p13 chr11: 93,400,633-93,400,633 CEP295
    nsv5269616copy number variation1nstd204human GRCh38.p13 chr11: 93,674,801-93,677,400 , GRCh37.p13 chr11: 93,407,967-93,410,566 CEP295
    nsv5183733mobile element insertion1nstd203human GRCh38 chr11: 93,694,748-93,694,767 , GRCh37.p13 chr11: 93,427,914-93,427,933 CEP295
    nsv4989175copy number variation1nstd200human GRCh38 chr11: 93,501,300-93,857,533 , GRCh37.p13 chr11: 93,234,466-93,590,699 VSTM5, SNORA18, 17 more genes
    nsv4971672copy number variation1nstd200human GRCh38 chr11: 93,709,531-93,709,688 , GRCh37.p13 chr11: 93,442,697-93,442,854 CEP295
    nsv4971671copy number variation1nstd200human GRCh38 chr11: 93,688,368-93,690,328 , GRCh37.p13 chr11: 93,421,534-93,423,494 CEP295
    nsv4971591copy number variation1nstd200human GRCh38 chr11: 91,285,470-94,799,390 , GRCh37.p13 chr11: 91,018,638-94,532,556 , LOC105369429, 53 more genes
    nsv4845767copy number variation1nstd200human GRCh37 chr11: 93,418,084-93,419,020 , GRCh38.p12 chr11: 93,684,918-93,685,854 CEP295
    nsv4839969copy number variation1nstd200human GRCh37 chr11: 91,018,638-94,532,556 , GRCh38.p12 chr11: 91,285,470-94,799,390 , MIR548L, 53 more genes
    nsv4834306copy number variation1nstd200human GRCh37 chr11: 93,421,534-93,423,494 , GRCh38.p12 chr11: 93,688,368-93,690,328 CEP295
    nsv4729052copy number variation1nstd102humanUncertain significance GRCh37 chr11: 92,615,227-93,592,229 , GRCh38.p12 chr11: 92,882,061-93,859,063 CEP295, RPL26P31, 26 more genes
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