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Items: 1 to 20 of 184

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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
    nsv6737845copy number variation1nstd229human GRCh38 chr3: 134,615,193-134,618,993 , GRCh37.p13 chr3: 134,334,035-134,337,835 CEP63, EPHB1, 1 more genes
    nsv6734332copy number variation1nstd229human GRCh38 chr3: 134,643,144-134,643,209 , GRCh37.p13 chr3: 134,361,986-134,362,051 EPHB1, KY, 1 more genes
    nsv6731577copy number variation1nstd229human GRCh38 chr3: 134,517,811-134,640,184 , GRCh37.p13 chr3: 134,236,653-134,359,026 CEP63, EPHB1, 1 more genes
    nsv6729156copy number variation1nstd229human GRCh38 chr3: 134,646,638-134,648,254 , GRCh37.p13 chr3: 134,365,480-134,367,096 KY, CEP63, 1 more genes
    nsv6728769copy number variation1nstd229human GRCh38 chr3: 134,632,816-134,640,294 , GRCh37.p13 chr3: 134,351,658-134,359,136 KY, CEP63, 1 more genes
    nsv6725354copy number variation1nstd229human GRCh38 chr3: 134,635,856-134,638,609 , GRCh37.p13 chr3: 134,354,698-134,357,451 EPHB1, CEP63, 1 more genes
    nsv6724640copy number variation1nstd229human GRCh38 chr3: 134,641,483-134,643,794 , GRCh37.p13 chr3: 134,360,325-134,362,636 KY, EPHB1, 1 more genes
    nsv6723947copy number variation1nstd229human GRCh38 chr3: 134,590,306-134,605,863 , GRCh37.p13 chr3: 134,309,148-134,324,705 KY, CEP63, 1 more genes
    nsv6721693copy number variation1nstd229human GRCh38 chr3: 134,601,772-134,611,032 , GRCh37.p13 chr3: 134,320,614-134,329,874 EPHB1, CEP63, 1 more genes
    nsv6720155copy number variation1nstd229human GRCh38 chr3: 134,509,227-135,423,554 , GRCh37.p13 chr3: 134,228,069-135,142,396 KY, LOC102724019, 7 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
    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
    nsv6371088copy number variation1nstd223human GRCh38 chr3: 134,631,501-134,632,300 , GRCh37.p13 chr3: 134,350,343-134,351,142 EPHB1, CEP63, 1 more genes
    nsv6369360copy number variation1nstd223human GRCh38 chr3: 134,632,101-134,634,900 , GRCh37.p13 chr3: 134,350,943-134,353,742 EPHB1, KY, 1 more genes
    nsv6368842copy number variation1nstd223human GRCh38 chr3: 134,517,811-134,640,184 , GRCh37.p13 chr3: 134,236,653-134,359,026 KY, EPHB1, 1 more genes
    nsv6295253copy number variation1nstd186human GRCh37 chr3: 134,361,997-134,362,051 , GRCh38.p12 chr3: 134,643,155-134,643,209 EPHB1, CEP63, 1 more genes
    nsv6156888copy number variation1nstd214human GRCh38 chr3: 134,643,144-134,643,208 , GRCh37.p13 chr3: 134,361,986-134,362,050 EPHB1, CEP63, 1 more genes
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