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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
    nsv5979328inversion1nstd209human GRCh38 chr19: 32,019,307-33,218,671 , GRCh37.p13 chr19: 32,510,213-33,709,577 , LRP3, 28 more genes
    nsv5946916copy number variation1nstd209human GRCh38 chr19: 32,707,774-32,816,785 , GRCh37.p13 chr19: 33,198,680-33,307,691 , TDRD12, 1 more genes
    nsv5881379copy number variation1nstd209human GRCh38 chr19: 32,707,743-32,728,421 , GRCh37.p13 chr19: 33,198,649-33,219,327 , TDRD12, 1 more genes
    nsv5515863copy number variation1nstd206human GRCh38 chr19: 32,712,374-32,712,425 , GRCh37.p13 chr19: 33,203,280-33,203,331 NUDT19
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020334copy number variation1nstd200human GRCh38 chr19: 32,692,105-32,692,187 , GRCh37.p13 chr19: 33,183,011-33,183,093 NUDT19
    nsv5020333copy number variation1nstd200human GRCh38 chr19: 32,685,700-32,689,935 , GRCh37.p13 chr19: 33,176,606-33,180,841 NUDT19
    nsv4861246copy number variation1nstd200human GRCh37 chr19: 33,186,158-33,195,193 , GRCh38.p12 chr19: 32,695,252-32,704,287 NUDT19
    nsv4861245copy number variation1nstd200human GRCh37 chr19: 33,176,606-33,180,841 , GRCh38.p12 chr19: 32,685,700-32,689,935 NUDT19
    nsv4679951copy number variation1nstd189human GRCh37.p13 chr19: 33,011,549-33,386,125 , GRCh38.p12 chr19: 32,520,643-32,895,219 , PDCD5, 11 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4268493copy number variation1nstd166human GRCh37.p13 chr19: 33,198,680-33,307,692 , GRCh38.p12 chr19: 32,707,774-32,816,786 , TDRD12, 1 more genes
    nsv4263952copy number variation1nstd166human GRCh37.p13 chr19: 33,203,000-33,210,000 , GRCh38.p12 chr19: 32,712,094-32,719,094 , NUDT19, 1 more genes
    nsv4256461copy number variation1nstd166human GRCh37.p13 chr19: 33,203,280-33,203,331 , GRCh38.p12 chr19: 32,712,374-32,712,425 NUDT19
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
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