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Items: 1 to 20 of 136

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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
    nsv6643322copy number variation1nstd229human GRCh38 chr1: 160,027,536-160,037,876 , GRCh37.p13 chr1: 159,997,326-160,007,666 PIGM, KCNJ10
    nsv6642974copy number variation1nstd229human GRCh38 chr1: 159,156,578-160,055,287 , GRCh37.p13 chr1: 159,126,368-160,025,077 RPL27AP2, ACKR1, 38 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
    nsv6332593copy number variation1nstd223human GRCh38 chr1: 160,028,248-160,029,109 , GRCh37.p13 chr1: 159,998,038-159,998,899 PIGM
    nsv6331564copy number variation1nstd223human GRCh38 chr1: 160,027,534-160,037,873 , GRCh37.p13 chr1: 159,997,324-160,007,663 PIGM, KCNJ10
    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
    nsv6245314mobile element insertion1nstd215human GRCh38 chr1: 160,026,263-160,026,263 , GRCh37.p13 chr1: 159,996,053-159,996,053 PIGM
    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
    nsv6133564copy number variation1nstd213human GRCh37 chr1: 159,330,000-160,200,001 , GRCh38.p12 chr1: 159,360,210-160,230,211 PEA15, OR10J1, 37 more genes
    nsv5427730copy number variation1nstd206human GRCh38 chr1: 160,027,536-160,037,873 , GRCh37.p13 chr1: 159,997,326-160,007,663 PIGM, KCNJ10
    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
    nsv5288847copy number variation1nstd204human GRCh38.p13 chr1: 160,026,500-160,029,810 , GRCh37.p13 chr1: 159,996,290-159,999,600 PIGM
    nsv4903948copy number variation1nstd200human GRCh38 chr1: 159,156,577-160,055,289 , GRCh37.p13 chr1: 159,126,367-160,025,079 , IGSF9, 40 more genes
    nsv4897722copy number variation1nstd200human GRCh38 chr1: 160,027,536-160,037,873 , GRCh37.p13 chr1: 159,997,326-160,007,663 PIGM, KCNJ10
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