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Items: 1 to 20 of 907

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148184copy number variation1nstd102humanPathogenic GRCh38 chr1: 243,221,458-248,919,110 , GRCh37.p13 chr1: 243,384,760-249,213,309 LOC105373271, LOC107985725, 153 more genes
    nsv7099273copy number variation1nstd231human GRCh38.p12 chr1: 248,590,032-248,805,400 , GRCh37 chr1: 248,753,333-249,099,599 OR2T10, OR2T11, 8 more genes
    nsv7098854copy number variation1nstd102humanPathogenic GRCh37 chr1: 245,704,069-249,212,562 , GRCh38.p12 chr1: 245,540,767-248,918,363 OR2X1P, OR14A2, 118 more genes
    nsv7038359inversion1nstd229human GRCh38 chr1: 248,566,967-248,724,069 , GRCh37.p13 chr1: 248,730,268-248,865,778 OR2T34, AHCYP8, 6 more genes
    nsv6676591copy number variation1nstd229human GRCh38 chr1: 247,742,306-248,679,100 , GRCh37.p13 chr1: 247,905,608-248,842,401 OR14A2, OR2T29, 50 more genes
    nsv6674276copy number variation1nstd229human GRCh38 chr1: 248,608,654-248,646,369 , GRCh37.p13 chr1: 248,771,955-248,809,670 OR2T11, OR2T10, 1 more genes
    nsv6665900copy number variation1nstd229human GRCh38 chr1: 247,656,440-248,785,565 , GRCh37.p13 chr1: 247,819,742-248,865,778 OR2X1P, OR3D1P, 60 more genes
    nsv6664871copy number variation1nstd229human GRCh38 chr1: 248,568,901-248,631,800 , GRCh37.p13 chr1: 248,732,202-248,795,101 OR2T10, OR2T34, 1 more genes
    nsv6662942copy number variation1nstd229human GRCh38 chr1: 248,564,501-248,631,100 , GRCh37.p13 chr1: 248,727,802-248,794,401 OR2T10, OR2T34, 1 more genes
    nsv6658822copy number variation1nstd229human GRCh38 chr1: 248,576,201-248,645,000 , GRCh37.p13 chr1: 248,739,502-248,808,301 OR2T11, OR2T10, 1 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636648copy number variation1nstd102humanPathogenic GRCh37 chr1: 239,910,960-249,224,684 , GRCh38.p12 chr1: 239,747,660-248,930,485 RFKP1, OR2T29, 206 more genes
    nsv6636282copy number variation1nstd102humanPathogenic GRCh37 chr1: 243,258,050-249,224,684 , GRCh38.p12 chr1: 243,094,748-248,930,485 AHCYP8, OR2M2, 154 more genes
    nsv6636061copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 242,045,197-249,212,668 , GRCh38.p12 chr1: 241,881,895-248,918,469 ADSS2, HNRNPU, 178 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6634340copy number variation1nstd102humanPathogenic GRCh37 chr1: 246,850,401-249,205,263 , GRCh38.p12 chr1: 246,687,099-248,911,064 OR14A2, VN1R16P, 106 more genes
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 OR2M4, KIF28P, 316 more genes
    nsv6626437copy number variation1nstd224human GRCh37 chr1: 248,496,863-248,877,789 , GRCh38.p12 chr1: 248,333,561-248,714,488 OR14C36, OR2T10, 19 more genes
    nsv6626362copy number variation3nstd224human GRCh37 chr1: 248,756,290-248,844,692 , GRCh38.p12 chr1: 248,592,989-248,681,391 OR2T10, OR14I1, 3 more genes
    nsv6626361copy number variation1nstd224human GRCh37 chr1: 248,684,976-248,790,246 , GRCh38.p12 chr1: 248,521,675-248,626,945 OR2AS1P, OR2T34, 5 more genes
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