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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096876copy number variation1nstd102humanUncertain significance GRCh37 chr2: 46,525,051-46,851,366 , GRCh38.p12 chr2: 46,297,912-46,624,227 TMEM247, CRIPT, 8 more genes
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6673010copy number variation1nstd229human GRCh38 chr2: 46,620,333-46,629,410 , GRCh37.p13 chr2: 46,847,472-46,856,549 CRIPT
    nsv6671921copy number variation1nstd229human GRCh38 chr2: 46,310,701-46,704,700 , GRCh37.p13 chr2: 46,537,840-46,931,839 SOCS5, LINC02583, 10 more genes
    nsv6667108copy number variation1nstd229human GRCh38 chr2: 46,596,979-46,622,620 , GRCh37.p13 chr2: 46,824,118-46,849,759 PIGF, CRIPT
    nsv6665632copy number variation1nstd229human GRCh38 chr2: 46,611,003-46,666,172 , GRCh37.p13 chr2: 46,838,142-46,893,311 LOC105374584, CRIPT, 1 more genes
    nsv6664781copy number variation1nstd229human GRCh38 chr2: 46,615,401-46,628,800 , GRCh37.p13 chr2: 46,842,540-46,855,939 PIGF, CRIPT
    nsv6662689copy number variation1nstd229human GRCh38 chr2: 46,629,356-46,632,974 , GRCh37.p13 chr2: 46,856,495-46,860,113 CRIPT
    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
    nsv6628307copy number variation1nstd224human GRCh37 chr2: 46,845,849-46,913,726 , GRCh38.p12 chr2: 46,618,710-46,686,587 LOC105374584, CRIPT
    nsv6348207copy number variation1nstd223human GRCh38 chr2: 46,627,575-46,628,241 , GRCh37.p13 chr2: 46,854,714-46,855,380 CRIPT
    nsv6346023copy number variation1nstd223human GRCh38 chr2: 46,612,600-46,618,149 , GRCh37.p13 chr2: 46,839,739-46,845,288 CRIPT, PIGF
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315248copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 46,844,310-46,845,911 , GRCh38.p12 chr2: 46,617,171-46,618,772 PIGF, CRIPT
    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
    nsv6251882mobile element insertion1nstd215human GRCh38 chr2: 46,623,880-46,623,880 , GRCh37.p13 chr2: 46,851,019-46,851,019 CRIPT
    nsv6134459copy number variation1nstd213human GRCh37 chr2: 40,080,000-50,820,001 , GRCh38.p12 chr2: 39,852,860-50,592,863 , BCYRN1, 149 more genes
    nsv6134458copy number variation2nstd213human GRCh37 chr2: 38,440,000-47,670,001 , GRCh38.p12 chr2: 38,212,858-47,442,862 ASS1P2, BCYRN1, 144 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
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