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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057129inversion1nstd229human GRCh38 chr2: 64,610,009-64,622,690 , GRCh37.p13 chr2: 64,837,143-64,849,824 LINC02579
    nsv7052460inversion1nstd229human GRCh38 chr2: 64,615,988-64,622,128 , GRCh37.p13 chr2: 64,843,122-64,849,262 LINC02579
    nsv7050849inversion1nstd229human GRCh38 chr2: 64,548,536-64,751,728 , GRCh37.p13 chr2: 64,775,670-64,978,862 SERTAD2, LOC105374775, 5 more genes
    nsv7041302inversion1nstd229human GRCh38 chr2: 64,610,006-64,618,518 , GRCh37.p13 chr2: 64,837,140-64,845,652 LINC02579
    nsv6673336copy number variation1nstd229human GRCh38 chr2: 64,608,630-64,612,285 , GRCh37.p13 chr2: 64,835,764-64,839,419 LINC02579
    nsv6671511copy number variation1nstd229human GRCh38 chr2: 64,611,223-64,616,331 , GRCh37.p13 chr2: 64,838,357-64,843,465 LINC02579
    nsv6661490copy number variation1nstd229human GRCh38 chr2: 64,210,609-64,960,847 , GRCh37.p13 chr2: 64,437,743-65,187,981 RN7SL211P, RNU6-100P, 23 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6551094inversion1nstd223human GRCh38 chr2: 64,078,330-67,334,177 , GRCh37.p13 chr2: 64,305,464-67,561,309 LINC01805, LINC02579, 59 more genes
    nsv6345338copy number variation1nstd223human GRCh38 chr2: 64,611,223-64,616,327 , GRCh37.p13 chr2: 64,838,357-64,843,461 LINC02579
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6134545copy number variation2nstd213human GRCh37 chr2: 47,990,000-75,070,001 , GRCh38.p12 chr2: 47,762,861-74,842,874 ACTG2, ACYP2, 438 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv5989750copy number variation1nstd212human GRCh38 chr2: 64,510,937-64,911,807 , GRCh37.p13 chr2: 64,738,071-65,138,941 , MIR4434, 14 more genes
    nsv5974385inversion1nstd209human GRCh38 chr2: 64,078,330-67,334,176 , GRCh37.p13 chr2: 64,305,464-67,561,308 , MEIS1, 63 more genes
    nsv5613325insertion1nstd207human GRCh38 chr2: 64,612,210-64,612,210 , GRCh37.p13 chr2: 64,839,344-64,839,344 LINC02579
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv4901609copy number variation1nstd200human GRCh38 chr2: 64,611,223-64,616,327 , GRCh37.p13 chr2: 64,838,357-64,843,461 LINC02579
    nsv4453429copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,536,353-65,793,944 , GRCh38.p12 chr2: 63,309,218-65,566,810 RPS4XP5, RNU6-548P, 48 more genes
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