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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7049104inversion1nstd229human GRCh38 chr3: 114,751,914-119,661,867 , GRCh37.p13 chr3: 114,470,761-119,380,714 LINC00901, EIF4E2P2, 50 more genes
    nsv6715053copy number variation1nstd229human GRCh38 chr3: 119,573,501-119,578,400 , GRCh37.p13 chr3: 119,292,348-119,297,247 ADPRH
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6704409copy number variation1nstd229human GRCh38 chr3: 119,468,099-119,806,079 , GRCh37.p13 chr3: 119,186,946-119,524,926 POPDC2, CFAP91, 13 more genes
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6637150copy number variation1nstd102humanUncertain significance GRCh37 chr3: 116,109,191-120,328,013 , GRCh38.p12 chr3: 116,390,344-120,609,166 LOC101926953, LOC105374058, 60 more genes
    nsv6628203copy number variation1nstd224human GRCh37 chr3: 119,301,255-119,312,613 , GRCh38.p12 chr3: 119,582,408-119,593,766 ADPRH
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
    nsv6362322copy number variation1nstd223human GRCh38 chr3: 119,573,547-119,578,453 , GRCh37.p13 chr3: 119,292,394-119,297,300 ADPRH
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv6071074insertion1nstd212human GRCh38 chr3: 119,582,500-119,582,500 , GRCh37.p13 chr3: 119,301,347-119,301,347 ADPRH
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919774copy number variation1nstd200human GRCh38 chr3: 119,573,547-119,578,453 , GRCh37.p13 chr3: 119,292,394-119,297,300 ADPRH
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv4082326copy number variation1nstd166human GRCh37.p13 chr3: 119,292,394-119,297,300 , GRCh38.p12 chr3: 119,573,547-119,578,453 ADPRH
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MYLK-AS2, RPL7AP11, 165 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577 POGLUT1, RN7SL397P, 141 more genes
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