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Items: 1 to 20 of 128

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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
    nsv7095484copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,309,679-160,320,060 , GRCh38.p12 chr1: 160,339,889-160,350,270 NCSTN, COPA
    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
    nsv6643333copy number variation1nstd229human GRCh38 chr1: 160,349,787-160,349,891 , GRCh37.p13 chr1: 160,319,577-160,319,681 NCSTN
    nsv6643242copy number variation1nstd229human GRCh38 chr1: 160,334,691-160,361,661 , GRCh37.p13 chr1: 160,304,481-160,331,451 NCSTN, COPA
    nsv6642897copy number variation1nstd229human GRCh38 chr1: 160,297,601-160,434,000 , GRCh37.p13 chr1: 160,267,391-160,403,790 LOC105371466, VANGL2, 6 more genes
    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
    nsv6310733copy number variation2nstd102humanUncertain significance GRCh37 chr1: 160,090,676-160,327,063 , GRCh38.p12 chr1: 160,120,886-160,357,273 SUMO1P3, NCSTN, 11 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
    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
    nsv5687135mobile element insertion1nstd211human GRCh38 chr1: 160,353,751-160,353,751 , GRCh37.p13 chr1: 160,323,541-160,323,541 NCSTN
    nsv5404988mobile element insertion1nstd206human GRCh38 chr1: 160,353,751-160,353,794 , GRCh37.p13 chr1: 160,323,541-160,323,584 NCSTN
    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
    nsv5073004mobile element insertion1nstd203human GRCh38 chr1: 160,359,170-160,359,203 , GRCh37.p13 chr1: 160,328,960-160,328,993 NCSTN
    nsv5065394mobile element insertion1nstd203human GRCh38 chr1: 160,353,739-160,353,751 , GRCh37.p13 chr1: 160,323,529-160,323,541 NCSTN
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