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Items: 1 to 20 of 498

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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
    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
    nsv7047206inversion1nstd229human GRCh38 chr1: 248,129,213-248,587,211 , GRCh37.p13 chr1: 248,292,515-248,750,512 OR2M5, OR2T2, 21 more genes
    nsv7045451inversion1nstd229human GRCh38 chr1: 248,394,224-248,564,628 , GRCh37.p13 chr1: 248,557,525-248,727,929 OR2T29, OR2T3, 9 more genes
    nsv7041109inversion1nstd229human GRCh38 chr1: 248,160,794-248,499,072 , GRCh37.p13 chr1: 248,324,096-248,662,373 OR2M2, OR2T12, 16 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
    nsv6675868copy number variation1nstd229human GRCh38 chr1: 247,840,153-248,617,375 , GRCh37.p13 chr1: 248,003,455-248,780,676 CLK3P2, OR2T7, 41 more genes
    nsv6670346copy number variation1nstd229human GRCh38 chr1: 247,948,628-248,526,413 , GRCh37.p13 chr1: 248,111,930-248,689,714 OR2T5, LOC105373279, 30 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
    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
    nsv6626359copy number variation1nstd224human GRCh37 chr1: 248,072,026-248,757,054 , GRCh38.p12 chr1: 247,908,724-248,593,753 OR2T7, OR2M5, 38 more genes
    nsv6626233copy number variation1nstd224human GRCh37 chr1: 248,343,343-248,616,236 , GRCh38.p12 chr1: 248,180,041-248,452,935 OR14C36, OR2T33, 10 more genes
    nsv6626003copy number variation1nstd224human GRCh37 chr1: 248,509,182-248,845,549 , GRCh38.p12 chr1: 248,345,880-248,682,248 OR2T7, OR2T29, 18 more genes
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