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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5448739copy number variation1nstd206human GRCh38 chr1: 247,661,000-248,560,600 , GRCh37.p13 chr1: 247,824,302-248,723,901 OR14A2, OR2AJ1, 49 more genes
    nsv5445146copy number variation1nstd206human GRCh38 chr1: 247,660,364-248,129,682 , GRCh37.p13 chr1: 247,823,666-248,292,984 OR13G1, OR9H1P, 27 more genes
    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
    nsv5216571copy number variation1nstd204human GRCh38.p13 chr1: 247,691,701-247,800,500 , GRCh37.p13 chr1: 247,855,003-247,963,802 OR1C1, OR14A2, 3 more genes
    nsv5211224copy number variation1nstd204human GRCh38.p13 chr1: 247,735,294-247,777,892 , GRCh37.p13 chr1: 247,898,596-247,941,194 OR14A2, OR14K1, 2 more genes
    nsv4904623copy number variation1nstd200human GRCh38 chr1: 247,555,500-248,007,565 , GRCh37.p13 chr1: 247,718,802-248,170,867 OR14L1, OR6R1P, 26 more genes
    nsv4891856copy number variation1nstd200human GRCh38 chr1: 247,729,413-247,776,917 , GRCh37.p13 chr1: 247,892,715-247,940,219 OR14A2, OR1C1, 2 more genes
    nsv4785782copy number variation1nstd200human GRCh37 chr1: 247,892,715-247,940,219 , GRCh38.p12 chr1: 247,729,413-247,776,917 OR1C1, OR14A2, 2 more genes
    nsv4728429copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 246,853,199-249,181,899 , GRCh38.p12 chr1: 246,689,897-248,887,700 ZNF124, TRIM58, 105 more genes
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 HLX-AS1, OPN3, 740 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 RNA5S8, NTPCR, 893 more genes
    nsv4594422copy number variation1nstd183human GRCh37 chr1: 247,835,393-248,292,032 , GRCh38.p12 chr1: 247,672,091-248,128,730 OR14A16, OR2T32P, 26 more genes
    nsv4581043copy number variation2nstd183human GRCh37 chr1: 247,839,012-248,403,244 , GRCh38.p12 chr1: 247,675,710-248,239,942 OR2L3, OR6F1, 30 more genes
    nsv4562404sequence alteration1nstd166human GRCh37.p13 chr1: 247,215,189-248,008,496 , GRCh38.p12 chr1: 247,051,887-247,845,194 , ZNF124, 39 more genes
    nsv4455005copy number variation1nstd102humanPathogenic GRCh37 chr1: 238,669,293-249,224,684 , GRCh38.p12 chr1: 238,505,993-248,930,485 ZNF731P, RNU6-947P, 212 more genes
    nsv4453906copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,582,580-249,224,684 , GRCh38.p12 chr1: 235,419,265-248,930,485 YWHAQP9, LOC107985747, 268 more genes
    nsv4453644copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,032,527-248,071,583 , GRCh38.p12 chr1: 246,869,225-247,908,281 LOC107985375, OR6F1, 44 more genes
    nsv4453436copy number variation1nstd102humanPathogenic GRCh37 chr1: 246,565,044-249,224,684 , GRCh38.p12 chr1: 246,401,742-248,930,485 LOC105373273, OR6F1, 113 more genes
    nsv4451356copy number variation1nstd102humanPathogenic GRCh37 chr1: 244,379,481-249,224,684 , GRCh38.p12 chr1: 244,216,179-248,930,485 RPL35AP6, LOC107985747, 140 more genes
    nsv4450593copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,576,587-248,688,602 , GRCh38.p12 chr1: 247,413,285-248,525,301 OR2T4, OR2T7, 57 more genes
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