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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7057605inversion1nstd229human GRCh38 chr1: 78,336,704-86,162,072 , GRCh37.p13 chr1: 78,802,388-86,627,755 LINC01712, LOC105378812, 74 more genes
    nsv7057036inversion1nstd229human GRCh38 chr1: 81,424,308-84,666,974 , GRCh37.p13 chr1: 81,889,993-85,132,657 SSX2IP, LINC01361, 29 more genes
    nsv7053103inversion1nstd229human GRCh38 chr1: 81,888,908-86,483,944 , GRCh37.p13 chr1: 82,354,593-86,949,627 C1orf52, DNAI3, 50 more genes
    nsv7050765inversion1nstd229human GRCh38 chr1: 80,818,811-84,572,591 , GRCh37.p13 chr1: 81,284,496-85,038,274 RPF1, LOC105378819, 32 more genes
    nsv7049591inversion1nstd229human GRCh38 chr1: 78,612,736-84,444,047 , GRCh37.p13 chr1: 79,078,421-84,909,730 RPS20P7, LINC02792, 44 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv7045562inversion1nstd229human GRCh38 chr1: 82,773,087-84,647,821 , GRCh37.p13 chr1: 83,238,770-85,113,504 LOC107985396, LINC01362, 22 more genes
    nsv6655362copy number variation1nstd229human GRCh38 chr1: 84,221,652-84,275,041 , GRCh37.p13 chr1: 84,687,335-84,740,724 NEDD8P1, PRKACB
    nsv6331060copy number variation1nstd223human GRCh38 chr1: 84,244,701-84,250,200 , GRCh37.p13 chr1: 84,710,384-84,715,883 NEDD8P1
    nsv6313647copy number variation1nstd102humanUncertain significance GRCh37 chr1: 84,084,511-84,921,911 , GRCh38.p12 chr1: 83,618,828-84,456,228 LINC01725, TXN2P1, 7 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv6290654copy number variation1nstd102humanUncertain significance GRCh37 chr1: 84,664,456-84,776,154 , GRCh38.p12 chr1: 84,198,773-84,310,471 SAMD13, NEDD8P1, 1 more genes
    nsv5211983copy number variation1nstd204human GRCh38.p13 chr1: 84,242,901-84,250,100 , GRCh37.p13 chr1: 84,708,584-84,715,783 , NEDD8P1
    nsv5071913mobile element insertion1nstd203human GRCh38 chr1: 84,245,104-84,245,118 , GRCh37.p13 chr1: 84,710,787-84,710,801 , NEDD8P1
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4873320inversion1nstd200human GRCh37 chr1: 84,115,994-85,474,764 , GRCh38.p12 chr1: 83,650,311-85,009,081 , SAMD13, 22 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
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