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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5686614mobile element insertion1nstd211human GRCh38 chr2: 207,710,197-207,710,197 , GRCh37.p13 chr2: 208,574,921-208,574,921 CCNYL1
    nsv5684289mobile element insertion2nstd211human GRCh38 chr2: 207,755,971-207,755,971 , GRCh37.p13 chr2: 208,620,695-208,620,695 FZD5, CCNYL1
    nsv5682982mobile element insertion1nstd211human GRCh38 chr2: 207,710,208-207,710,208 , GRCh37.p13 chr2: 208,574,932-208,574,932 CCNYL1
    nsv5680355mobile element insertion1nstd211human GRCh38 chr2: 207,718,743-207,718,743 , GRCh37.p13 chr2: 208,583,467-208,583,467 CCNYL1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5556089sequence alteration1nstd206human GRCh38 chr2: 207,609,176-207,721,927 , GRCh37.p13 chr2: 208,473,900-208,586,651 METTL21A, CCNYL1, 4 more genes
    nsv5447785copy number variation1nstd206human GRCh38 chr2: 207,611,618-207,722,000 , GRCh37.p13 chr2: 208,476,342-208,586,724 METTL21A, CCNYL1, 4 more genes
    nsv5435115copy number variation1nstd206human GRCh38 chr2: 207,722,681-207,722,976 , GRCh37.p13 chr2: 208,587,405-208,587,700 CCNYL1
    nsv5412535mobile element insertion1nstd206human GRCh38 chr2: 207,755,971-207,756,022 , GRCh37.p13 chr2: 208,620,695-208,620,746 FZD5, CCNYL1
    nsv5403968mobile element insertion1nstd206human GRCh38 chr2: 207,718,743-207,718,794 , GRCh37.p13 chr2: 208,583,467-208,583,518 CCNYL1
    nsv5063504mobile element insertion1nstd203human GRCh38 chr2: 207,755,954-207,755,971 , GRCh37.p13 chr2: 208,620,678-208,620,695 CCNYL1, FZD5
    nsv5033412inversion1nstd200human GRCh38 chr2: 206,107,842-207,979,103 , GRCh37.p13 chr2: 206,972,566-208,843,827 ATP5POP1, MIR2355, 39 more genes
    nsv4913873copy number variation1nstd200human GRCh38 chr2: 207,745,777-207,748,216 , GRCh37.p13 chr2: 208,610,501-208,612,940 CCNYL1
    nsv4876881inversion1nstd200human GRCh37 chr2: 206,972,566-208,843,827 , GRCh38.p12 chr2: 206,107,842-207,979,103 CREB1, RN7SKP260, 39 more genes
    nsv4804575copy number variation1nstd200human GRCh37 chr2: 208,610,501-208,612,940 , GRCh38.p12 chr2: 207,745,777-207,748,216 CCNYL1
    nsv4795703copy number variation1nstd200human GRCh37 chr2: 208,603,216-208,604,196 , GRCh38.p12 chr2: 207,738,492-207,739,472 CCNYL1
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728545copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,445,619-212,580,788 , GRCh38.p12 chr2: 203,580,896-211,716,063 FASTKD2, MYL6BP1, 110 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4568419mobile element insertion1nstd166human GRCh37.p13 chr2: 208,574,341-208,574,341 , GRCh38.p12 chr2: 207,709,617-207,709,617 CCNYL1
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