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Items: 1 to 20 of 718

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096934copy number variation1nstd102humanPathogenic GRCh37 chr3: 134,225,951-134,251,742 , GRCh38.p12 chr3: 134,507,109-134,532,900 DPPA4P2, CEP63
    nsv7052538inversion1nstd229human GRCh38 chr3: 134,489,784-134,489,839 , GRCh37.p13 chr3: 134,208,626-134,208,681 CEP63
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7051204inversion1nstd229human GRCh38 chr3: 134,736,243-134,739,619 , GRCh37.p13 chr3: 134,455,085-134,458,461 EPHB1, CEP63
    nsv7044646inversion1nstd229human GRCh38 chr3: 134,759,837-134,774,704 , GRCh37.p13 chr3: 134,478,679-134,493,546 EPHB1, CEP63
    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
    nsv6736126copy number variation1nstd229human GRCh38 chr3: 134,511,932-134,517,800 , GRCh37.p13 chr3: 134,230,774-134,236,642 CEP63
    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
    nsv6734046copy number variation1nstd229human GRCh38 chr3: 134,528,691-134,536,491 , GRCh37.p13 chr3: 134,247,533-134,255,333 CEP63
    nsv6732173copy number variation1nstd229human GRCh38 chr3: 134,771,975-134,777,634 , GRCh37.p13 chr3: 134,490,817-134,496,476 CEP63, EPHB1
    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
    nsv6731300copy number variation1nstd229human GRCh38 chr3: 134,755,381-134,762,126 , GRCh37.p13 chr3: 134,474,223-134,480,968 EPHB1, CEP63
    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
    nsv6728990copy number variation1nstd229human GRCh38 chr3: 134,566,924-134,570,033 , GRCh37.p13 chr3: 134,285,766-134,288,875 CEP63
    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
    nsv6726356copy number variation1nstd229human GRCh38 chr3: 134,567,501-134,581,600 , GRCh37.p13 chr3: 134,286,343-134,300,442 CEP63
    nsv6725974copy number variation1nstd229human GRCh38 chr3: 134,726,657-134,741,918 , GRCh37.p13 chr3: 134,445,499-134,460,760 EPHB1, CEP63
    nsv6725956copy number variation1nstd229human GRCh38 chr3: 134,666,673-134,680,009 , GRCh37.p13 chr3: 134,385,515-134,398,851 CEP63, EPHB1
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