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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5875732copy number variation1nstd209human GRCh38 chr1: 178,037,696-178,037,745 , GRCh37.p13 chr1: 178,006,831-178,006,880 CRYZL2P, CRYZL2P-SEC16B
    nsv5715340mobile element insertion2nstd211human GRCh38 chr1: 178,025,123-178,025,123 , GRCh37.p13 chr1: 177,994,258-177,994,258 CRYZL2P-SEC16B, CRYZL2P
    nsv5690532mobile element insertion2nstd211human GRCh38 chr1: 178,017,216-178,017,216 , GRCh37.p13 chr1: 177,986,351-177,986,351 CRYZL2P, CRYZL2P-SEC16B
    nsv5615205insertion1nstd207human GRCh38 chr1: 178,017,199-178,017,199 , GRCh37.p13 chr1: 177,986,334-177,986,334 CRYZL2P-SEC16B, CRYZL2P
    nsv5572233copy number variation1nstd207human GRCh38 chr1: 178,037,696-178,037,745 , GRCh37.p13 chr1: 178,006,831-178,006,880 CRYZL2P-SEC16B, CRYZL2P
    nsv5559700mobile element insertion1nstd206human GRCh38 chr1: 178,025,123-178,025,174 , GRCh37.p13 chr1: 177,994,258-177,994,309 CRYZL2P-SEC16B, CRYZL2P
    nsv5431983copy number variation1nstd206human GRCh38 chr1: 178,009,576-178,031,899 , GRCh37.p13 chr1: 177,978,711-178,001,034 CRYZL2P-SEC16B, CRYZL2P
    nsv5419807copy number variation1nstd206human GRCh38 chr1: 178,037,696-178,037,746 , GRCh37.p13 chr1: 178,006,831-178,006,881 CRYZL2P, CRYZL2P-SEC16B
    nsv5396694mobile element insertion1nstd206human GRCh38 chr1: 178,017,216-178,017,267 , GRCh37.p13 chr1: 177,986,351-177,986,402 CRYZL2P-SEC16B, CRYZL2P
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5288003copy number variation1nstd204human GRCh37.p13 chr1: 177,784,611-178,417,549 , GRCh38.p13 chr1: 177,815,476-178,448,414 RASAL2, SEC16B, 6 more genes
    nsv5219635copy number variation1nstd204human GRCh37.p13 chr1: 177,784,636-178,131,135 , GRCh38.p13 chr1: 177,815,501-178,162,000 RASAL2, SEC16B, 4 more genes
    nsv5217333copy number variation1nstd204human GRCh38.p13 chr1: 178,035,300-178,048,328 , GRCh37.p13 chr1: 178,004,435-178,017,463 CRYZL2P-SEC16B, CRYZL2P
    nsv5208530copy number variation1nstd204human GRCh38.p13 chr1: 178,007,821-178,054,068 , GRCh37.p13 chr1: 177,976,956-178,023,203 CRYZL2P-SEC16B, CRYZL2P
    nsv5079993mobile element insertion1nstd203human GRCh38 chr1: 178,017,200-178,017,216 , GRCh37.p13 chr1: 177,986,335-177,986,351 CRYZL2P-SEC16B, CRYZL2P
    nsv5062876mobile element insertion1nstd203human GRCh38 chr1: 178,017,199-178,017,216 , GRCh37.p13 chr1: 177,986,334-177,986,351 CRYZL2P, CRYZL2P-SEC16B
    nsv4904052copy number variation1nstd200human GRCh38 chr1: 178,024,082-178,081,777 , GRCh37.p13 chr1: 177,993,217-178,050,912 CRYZL2P-SEC16B, CRYZL2P
    nsv4904046copy number variation1nstd200human GRCh38 chr1: 176,794,951-178,186,897 , GRCh37.p13 chr1: 176,764,087-178,156,032 LINC01741, RASAL2-AS1, 11 more genes
    nsv4898194copy number variation1nstd200human GRCh38 chr1: 178,013,929-178,021,419 , GRCh37.p13 chr1: 177,983,064-177,990,554 CRYZL2P, CRYZL2P-SEC16B
    nsv4781282copy number variation1nstd200human GRCh37 chr1: 176,764,087-178,156,032 , GRCh38.p12 chr1: 176,794,951-178,186,897 CRYZL2P, ASTN1, 11 more genes
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