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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 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
    nsv6643251copy number variation1nstd229human GRCh38 chr1: 160,601,953-160,606,252 , GRCh37.p13 chr1: 160,571,743-160,576,042 SLAMF1
    nsv6637035copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,778,364-160,770,515 , GRCh38.p12 chr1: 159,808,574-160,800,725 PEX19, SLAMF8, 43 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
    nsv6316415copy number variation1nstd223human GRCh38 chr1: 160,601,953-160,606,249 , GRCh37.p13 chr1: 160,571,743-160,576,039 SLAMF1
    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
    nsv6307672mobile element insertion1nstd186human GRCh37 chr1: 160,578,714-160,578,750 , GRCh38.p12 chr1: 160,608,924-160,608,960 SLAMF1
    nsv6133932copy number variation1nstd213human GRCh37 chr1: 160,280,000-160,600,001 , GRCh38.p12 chr1: 160,310,210-160,630,211 COPA, NCSTN, 10 more genes
    nsv6133931copy number variation1nstd213human GRCh37 chr1: 159,860,000-160,630,001 , GRCh38.p12 chr1: 159,890,210-160,660,211 COPA, NHLH1, 33 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
    nsv5724763mobile element insertion1nstd211human GRCh38 chr1: 160,608,909-160,608,909 , GRCh37.p13 chr1: 160,578,699-160,578,699 SLAMF1
    nsv5557747mobile element insertion1nstd206human GRCh38 chr1: 160,608,924-160,608,960 , GRCh37.p13 chr1: 160,578,714-160,578,750 SLAMF1
    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
    nsv5200016mobile element insertion1nstd203human GRCh38 chr1: 160,608,909-160,608,924 , GRCh37.p13 chr1: 160,578,699-160,578,714 SLAMF1
    nsv5075880mobile element insertion1nstd203human GRCh38 chr1: 160,621,269-160,621,280 , GRCh37.p13 chr1: 160,591,059-160,591,070 SLAMF1
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