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Items: 1 to 20 of 135

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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
    nsv5940027copy number variation1nstd209human GRCh38 chr19: 32,031,680-32,031,731 , GRCh37.p13 chr19: 32,522,586-32,522,637 LINC01533, LINC01837
    nsv5937157copy number variation1nstd209human GRCh38 chr19: 32,048,466-32,048,521 , GRCh37.p13 chr19: 32,539,372-32,539,427 LINC01533, LINC01837
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020311copy number variation1nstd200human GRCh38 chr19: 32,045,139-32,046,763 , GRCh37.p13 chr19: 32,536,045-32,537,669 LINC01837, LINC01533
    nsv4861230copy number variation1nstd200human GRCh37 chr19: 32,536,047-32,537,669 , GRCh38.p12 chr19: 32,045,141-32,046,763 LINC01837, LINC01533
    nsv4729927copy number variation1nstd102humanUncertain significance GRCh37 chr19: 32,361,430-32,764,618 , GRCh38.p12 chr19: 31,870,524-32,273,712 LOC105376899, RNA5SP472, 4 more genes
    nsv4715921copy number variation1nstd195human GRCh37 chr19: 32,145,451-33,022,201 , GRCh38.p12 chr19: 31,654,545-32,531,295 , DPY19L3, 12 more genes
    nsv4712385copy number variation1nstd195human GRCh37 chr19: 32,145,451-33,078,501 , GRCh38.p12 chr19: 31,654,545-32,587,595 , DPY19L3-DT, 13 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
    nsv4262304copy number variation1nstd166human GRCh37.p13 chr19: 32,522,588-32,522,638 , GRCh38.p12 chr19: 32,031,682-32,031,732 LINC01533, LINC01837
    nsv4259048copy number variation1nstd166human GRCh37.p13 chr19: 32,536,054-32,537,669 , GRCh38.p12 chr19: 32,045,148-32,046,763 LINC01837, LINC01533
    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
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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