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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7095400copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,277,234-13,249,220 , GRCh38.p12 chr19: 11,166,558-13,138,406 ZNF627, RGL3, 120 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv7015659copy number variation1nstd229human GRCh38 chr19: 11,824,251-12,016,223 , GRCh37.p13 chr19: 11,935,066-12,127,038 VN2R21P, VN2R14P, 11 more genes
    nsv7014607copy number variation1nstd229human GRCh38 chr19: 11,858,339-11,869,168 , GRCh37.p13 chr19: 11,969,154-11,979,983 ZNF439
    nsv7013737copy number variation1nstd229human GRCh38 chr19: 11,855,601-11,862,600 , GRCh37.p13 chr19: 11,966,416-11,973,415 ZNF439
    nsv7012881copy number variation1nstd229human GRCh38 chr19: 11,835,280-11,854,633 , GRCh37.p13 chr19: 11,946,095-11,965,448 ZNF439, VN2R13P, 1 more genes
    nsv7005768copy number variation1nstd229human GRCh38 chr19: 11,808,748-11,848,070 , GRCh37.p13 chr19: 11,919,563-11,958,885 ZNF439, ZNF491, 2 more genes
    nsv7003607copy number variation1nstd229human GRCh38 chr19: 11,868,376-11,895,060 , GRCh37.p13 chr19: 11,979,191-12,005,875 ZNF69, VN2R14P, 1 more genes
    nsv7003321copy number variation1nstd229human GRCh38 chr19: 11,869,702-11,872,814 , GRCh37.p13 chr19: 11,980,517-11,983,629 ZNF439, VN2R14P
    nsv7002989copy number variation1nstd229human GRCh38 chr19: 11,851,249-11,855,917 , GRCh37.p13 chr19: 11,962,064-11,966,732 ZNF439
    nsv6999294copy number variation1nstd229human GRCh38 chr19: 11,836,894-12,128,680 , GRCh37.p13 chr19: 11,947,709-12,239,495 ZNF700, VN2R21P, 17 more genes
    nsv6637950copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,753,820-12,272,905 , GRCh38.p12 chr19: 11,643,005-12,162,090 ZNF433, ZNF878, 29 more genes
    nsv6624673copy number variation1nstd224human GRCh37 chr19: 11,915,185-12,061,016 , GRCh38.p12 chr19: 11,804,370-11,950,201 ZNF69, ZNF700, 7 more genes
    nsv6599683inversion1nstd223human GRCh38 chr19: 11,864,910-11,865,713 , GRCh37.p13 chr19: 11,975,725-11,976,528 ZNF439
    nsv6599583inversion1nstd223human GRCh38 chr19: 11,864,601-11,865,889 , GRCh37.p13 chr19: 11,975,416-11,976,704 ZNF439
    nsv6529344copy number variation1nstd223human GRCh38 chr19: 11,857,999-11,860,200 , GRCh37.p13 chr19: 11,968,814-11,971,015 ZNF439
    nsv6529155copy number variation1nstd223human GRCh38 chr19: 11,863,509-11,864,702 , GRCh37.p13 chr19: 11,974,324-11,975,517 ZNF439
    nsv6524015copy number variation1nstd223human GRCh38 chr19: 11,867,527-11,867,893 , GRCh37.p13 chr19: 11,978,342-11,978,708 ZNF439
    nsv6521792copy number variation1nstd223human GRCh38 chr19: 11,808,748-11,848,070 , GRCh37.p13 chr19: 11,919,563-11,958,885 ZNF440, ZNF439, 2 more genes
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