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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6726808copy number variation1nstd229human GRCh38 chr3: 134,478,901-134,481,400 , GRCh37.p13 chr3: 134,197,743-134,200,242 ANAPC13
    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
    nsv6634336copy number variation1nstd102humanPathogenic GRCh37 chr3: 133,998,370-134,678,040 , GRCh38.p12 chr3: 134,279,528-134,959,198 MIR6827, EPHB1, 14 more genes
    nsv6134404copy number variation1nstd213human GRCh37 chr3: 133,870,000-134,410,001 , GRCh38.p12 chr3: 134,151,156-134,691,159 EPHB1, RYK, 13 more genes
    nsv6134403copy number variation1nstd213human GRCh37 chr3: 133,600,000-135,410,001 , GRCh38.p12 chr3: 133,881,156-135,691,159 RAB6B, KY, 23 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5317281copy number variation1nstd204human GRCh37.p13 chr3: 134,199,824-134,236,320 , GRCh38.p13 chr3: 134,480,982-134,517,478 ANAPC13, CEP63, 1 more genes
    nsv5225397copy number variation1nstd204human GRCh38.p13 chr3: 134,480,472-134,517,551 , GRCh37.p13 chr3: 134,199,314-134,236,393 CEP63, DPPA4P2, 1 more genes
    nsv5087000mobile element insertion1nstd203human GRCh38 chr3: 134,480,234-134,480,251 , GRCh37.p13 chr3: 134,199,076-134,199,093 ANAPC13
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4791129copy number variation1nstd200human GRCh37 chr3: 134,199,830-134,236,318 , GRCh38.p12 chr3: 134,480,988-134,517,476 ANAPC13, CEP63, 1 more genes
    nsv4679565copy number variation1nstd189human GRCh37.p13 chr3: 134,199,107-134,344,953 , GRCh38.p12 chr3: 134,480,265-134,626,111 EPHB1, ANAPC13, 3 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4103178copy number variation1nstd166human GRCh37.p13 chr3: 134,186,242-134,281,860 , GRCh38.p12 chr3: 134,467,400-134,563,018 ANAPC13, CEP63, 1 more genes
    nsv4096852copy number variation1nstd166human GRCh37.p13 chr3: 134,197,334-134,197,392 , GRCh38.p12 chr3: 134,478,492-134,478,550 ANAPC13
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
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