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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077519inversion1nstd229human GRCh38 chr12: 86,495,718-92,133,299 , GRCh37.p13 chr12: 86,889,495-92,527,075 CEP290, MIR3059, 60 more genes
    nsv7076646inversion1nstd229human GRCh38 chr12: 91,058,610-91,118,456 , GRCh37.p13 chr12: 91,452,387-91,512,233 LUM
    nsv7072688inversion1nstd229human GRCh38 chr12: 91,101,929-91,118,736 , GRCh37.p13 chr12: 91,495,706-91,512,513 LUM
    nsv7060010inversion1nstd229human GRCh38 chr12: 86,085,575-91,207,469 , GRCh37.p13 chr12: 86,479,353-91,601,246 POC1B, C12orf50, 55 more genes
    nsv6936560copy number variation1nstd229human GRCh38 chr12: 91,109,002-91,111,396 , GRCh37.p13 chr12: 91,502,779-91,505,173 LUM
    nsv6934679copy number variation1nstd229human GRCh38 chr12: 90,974,160-91,138,037 , GRCh37.p13 chr12: 91,367,937-91,531,814 KERA, EPYC, 1 more genes
    nsv6927695copy number variation1nstd229human GRCh38 chr12: 90,167,236-91,253,354 , GRCh37.p13 chr12: 90,561,013-91,647,131 LOC105369895, EPYC, 8 more genes
    nsv6922681copy number variation1nstd229human GRCh38 chr12: 91,104,319-91,108,116 , GRCh37.p13 chr12: 91,498,096-91,501,893 LUM
    nsv6922173copy number variation1nstd229human GRCh38 chr12: 90,850,701-91,231,900 , GRCh37.p13 chr12: 91,244,478-91,625,677 LINC00615, CCER1, 4 more genes
    nsv6921992copy number variation1nstd229human GRCh38 chr12: 91,044,176-91,486,796 , GRCh37.p13 chr12: 91,437,953-91,880,573 DCN, LOC105369896, 4 more genes
    nsv6621897copy number variation1nstd224human GRCh37 chr12: 90,560,078-91,630,155 , GRCh38.p12 chr12: 90,166,301-91,236,378 LINC00615, LINC02822, 8 more genes
    nsv6621758copy number variation1nstd224human GRCh37 chr12: 90,562,017-91,630,155 , GRCh38.p12 chr12: 90,168,240-91,236,378 DCN, EPYC, 8 more genes
    nsv6621632copy number variation1nstd224human GRCh37 chr12: 91,469,750-91,506,953 , GRCh38.p12 chr12: 91,075,973-91,113,176 LUM
    nsv6313949copy number variation1nstd102humanUncertain significance GRCh37 chr12: 91,073,628-92,829,926 , GRCh38.p12 chr12: 90,679,851-92,436,150 LOC105369896, LINC00615, 20 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132715copy number variation1nstd213human GRCh37 chr12: 84,440,000-93,800,001 , GRCh38.p12 chr12: 84,046,221-93,406,225 , BTG1, 102 more genes
    nsv6132447copy number variation1nstd213human GRCh37 chr12: 91,370,000-91,570,001 , GRCh38.p12 chr12: 90,976,223-91,176,224 DCN, EPYC, 2 more genes
    nsv5940510copy number variation1nstd209human GRCh38 chr12: 91,109,722-91,219,266 , GRCh37.p13 chr12: 91,503,499-91,613,043 LUM, DCN
    nsv5860009copy number variation1nstd209human GRCh38 chr12: 91,097,304-91,102,124 , GRCh37.p13 chr12: 91,491,081-91,495,901 LUM
    nsv5858920copy number variation1nstd209human GRCh38 chr12: 91,109,630-91,114,129 , GRCh37.p13 chr12: 91,503,407-91,507,906 LUM
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