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Items: 1 to 20 of 117

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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
    nsv6643330copy number variation1nstd229human GRCh38 chr1: 160,265,701-160,317,400 , GRCh37.p13 chr1: 160,235,491-160,287,190 PEX19, RPSAP18, 3 more genes
    nsv6642899copy number variation1nstd229human GRCh38 chr1: 160,314,346-160,318,802 , GRCh37.p13 chr1: 160,284,136-160,288,592 COPA, SUMO1P3
    nsv6642898copy number variation1nstd229human GRCh38 chr1: 160,310,801-160,318,600 , GRCh37.p13 chr1: 160,280,591-160,288,390 COPA, SUMO1P3
    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
    nsv5416418copy number variation1nstd206human GRCh38 chr1: 160,314,346-160,318,795 , GRCh37.p13 chr1: 160,284,136-160,288,585 COPA, SUMO1P3
    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
    nsv4897731copy number variation1nstd200human GRCh38 chr1: 160,317,123-160,317,216 , GRCh37.p13 chr1: 160,286,913-160,287,006 SUMO1P3, COPA
    nsv4784441copy number variation1nstd200human GRCh37 chr1: 160,286,913-160,287,006 , GRCh38.p12 chr1: 160,317,123-160,317,216 SUMO1P3, COPA
    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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