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Items: 1 to 20 of 124

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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
    nsv7057021inversion1nstd229human GRCh38 chr1: 159,807,893-159,974,169 , GRCh37.p13 chr1: 159,777,683-159,943,959 MIR4259, TAGLN2, 10 more genes
    nsv7046668inversion1nstd229human GRCh38 chr1: 158,867,577-159,867,183 , GRCh37.p13 chr1: 158,837,367-159,836,973 PYHIN1, ACKR1, 35 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
    nsv6643318copy number variation1nstd229human GRCh38 chr1: 159,861,712-159,867,892 , GRCh37.p13 chr1: 159,831,502-159,837,682 LOC107985216, VSIG8
    nsv6643095copy number variation1nstd229human GRCh38 chr1: 159,463,702-160,016,243 , GRCh37.p13 chr1: 159,433,492-159,986,033 LINC01133, LOC105371464, 22 more genes
    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
    nsv6334619copy number variation1nstd223human GRCh38 chr1: 159,474,182-159,947,925 , GRCh37.p13 chr1: 159,443,972-159,917,715 OR10J6P, DUSP23, 19 more genes
    nsv6326223copy number variation1nstd223human GRCh38 chr1: 159,849,053-159,897,513 , GRCh37.p13 chr1: 159,818,843-159,867,303 VSIG8, SNHG28, 2 more genes
    nsv6325573copy number variation1nstd223human GRCh38 chr1: 159,463,696-160,016,249 , GRCh37.p13 chr1: 159,433,486-159,986,039 CRPP1, FCRL6, 22 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
    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
    nsv5563779sequence alteration1nstd206human GRCh38 chr1: 159,807,892-159,974,165 , GRCh37.p13 chr1: 159,777,682-159,943,955 , TAGLN2, 11 more genes
    nsv5419486copy number variation1nstd206human GRCh38 chr1: 159,857,987-159,858,059 , GRCh37.p13 chr1: 159,827,777-159,827,849 VSIG8, LOC107985216
    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
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