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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095487copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,279,609-161,751,809 , GRCh38.p12 chr1: 161,309,819-161,782,019 FCGR2C, RNU6-481P, 56 more genes
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6637016copy number variation1nstd102humanUncertain significance GRCh37 chr1: 161,207,985-161,437,998 , GRCh38.p12 chr1: 161,238,195-161,468,208 TRL-CAG1-4, TRD-GTC2-2, 34 more genes
    nsv6625854copy number variation1nstd224human GRCh37 chr1: 161,272,441-161,479,745 , GRCh38.p12 chr1: 161,302,651-161,509,955 SDHC, CFAP126, 35 more genes
    nsv6625853copy number variation1nstd224human GRCh37 chr1: 161,239,471-161,596,027 , GRCh38.p12 chr1: 161,269,681-161,626,237 FCGR3A, SDHC, 51 more genes
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 USF1, TRE-CTC1-3, 161 more genes
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6297573copy number variation1nstd186human GRCh37 chr1: 161,415,490-161,640,377 , GRCh38.p12 chr1: 161,445,700-161,670,587 TRE-CTC1-5, TRE-CTC1-2, 34 more genes
    nsv6138675copy number variation1nstd206human GRCh38 chr1: 161,445,700-161,670,587 , GRCh37.p13 chr1: 161,415,490-161,640,377 TRG-GCC4-1, TRG-GCC2-1, 34 more genes
    nsv6133743copy number variation1nstd213human GRCh37 chr1: 160,920,000-161,500,001 , GRCh38.p12 chr1: 160,950,210-161,530,211 HSPA6, NIT1, 67 more genes
    nsv6133742copy number variation1nstd213human GRCh37 chr1: 158,430,000-161,510,001 , GRCh38.p12 chr1: 158,460,210-161,540,211 APCS, FCER1A, 174 more genes
    nsv6133741copy number variation1nstd213human GRCh37 chr1: 158,390,000-161,480,001 , GRCh38.p12 chr1: 158,420,210-161,510,211 ATP1A4, CD48, 169 more genes
    nsv6133740copy number variation1nstd213human GRCh37 chr1: 158,330,000-161,530,001 , GRCh38.p12 chr1: 158,360,210-161,560,211 ATP1A2, ATP1A4, 178 more genes
    nsv5981430copy number variation1nstd212human GRCh38 chr1: 161,443,100-161,472,801 , GRCh37.p13 chr1: 161,412,890-161,442,591 TRL-CAG1-2, TRD-GTC2-4, 18 more genes
    nsv5672439inversion1nstd207human GRCh38 chr1: 161,373,416-161,476,251 , GRCh37.p13 chr1: 161,343,206-161,446,041 RRM2P2, SDHC, 30 more genes
    nsv5431559copy number variation1nstd206human GRCh38 chr1: 161,441,000-161,472,100 , GRCh37.p13 chr1: 161,410,790-161,441,890 TRL-CAG1-1, TRG-TCC2-4, 20 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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