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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053833inversion1nstd229human GRCh38 chr1: 28,579,668-28,579,708 , GRCh37.p13 chr1: 28,906,180-28,906,220 SNORA61, SNHG12, 2 more genes
    nsv7045620inversion1nstd229human GRCh38 chr1: 28,480,864-28,632,617 , GRCh37.p13 chr1: 28,807,376-28,959,129 SNORA61, SNORA16A, 13 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv7040370inversion1nstd229human GRCh38 chr1: 28,324,061-28,688,380 , GRCh37.p13 chr1: 28,650,572-29,014,892 PHACTR4, SNORD99, 17 more genes
    nsv6648336copy number variation1nstd229human GRCh38 chr1: 28,579,727-28,583,069 , GRCh37.p13 chr1: 28,906,239-28,909,581 SNORA16A, SNORA61, 2 more genes
    nsv6648335copy number variation1nstd229human GRCh38 chr1: 28,579,558-28,579,902 , GRCh37.p13 chr1: 28,906,070-28,906,414 SNHG12, SNORA44, 2 more genes
    nsv6648334copy number variation1nstd229human GRCh38 chr1: 28,576,199-28,658,409 , GRCh37.p13 chr1: 28,902,711-28,984,921 SNORA61, TAF12-DT, 8 more genes
    nsv6648333copy number variation1nstd229human GRCh38 chr1: 28,558,354-28,590,252 , GRCh37.p13 chr1: 28,884,866-28,916,764 SNHG12, SNORD99, 4 more genes
    nsv6648160copy number variation1nstd229human GRCh38 chr1: 28,455,818-28,753,520 , GRCh37.p13 chr1: 28,782,329-29,080,032 GMEB1, YTHDF2, 17 more genes
    nsv6332278copy number variation1nstd223human GRCh38 chr1: 28,486,426-28,604,771 , GRCh37.p13 chr1: 28,812,938-28,931,283 SNORA73B, SNORA16A, 12 more genes
    nsv6324231copy number variation1nstd223human GRCh38 chr1: 28,441,490-28,620,687 , GRCh37.p13 chr1: 28,768,001-28,947,199 RNU6ATAC27P, SNORA73A, 13 more genes
    nsv6322009copy number variation1nstd223human GRCh38 chr1: 28,571,798-28,599,590 , GRCh37.p13 chr1: 28,898,310-28,926,102 TRNAU1AP, SNHG12, 5 more genes
    nsv6321067copy number variation1nstd223human GRCh38 chr1: 28,578,023-28,580,113 , GRCh37.p13 chr1: 28,904,535-28,906,625 TRNAU1AP, SNHG12, 4 more genes
    nsv6319572copy number variation1nstd223human GRCh38 chr1: 28,455,818-28,753,520 , GRCh37.p13 chr1: 28,782,329-29,080,032 RAB42, SNORA44, 17 more genes
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6290388copy number variation1nstd102humanUncertain significance GRCh37 chr1: 28,493,687-29,242,679 , GRCh38.p12 chr1: 28,167,176-28,916,167 SNORA16A, MED18, 24 more genes
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv5876686copy number variation1nstd209human GRCh38 chr1: 28,579,555-28,579,901 , GRCh37.p13 chr1: 28,906,067-28,906,413 SNHG12, SNORA44, 2 more genes
    nsv5433866copy number variation1nstd206human GRCh38 chr1: 28,578,681-28,579,531 , GRCh37.p13 chr1: 28,905,193-28,906,043 TRNAU1AP, SNHG12, 4 more genes
    nsv5432511copy number variation1nstd206human GRCh38 chr1: 28,544,028-28,585,801 , GRCh37.p13 chr1: 28,870,540-28,912,313 TRNAU1AP, SNHG12, 4 more genes
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