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Items: 1 to 20 of 441

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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
    nsv7099272copy number variation1nstd231human GRCh38.p12 chr1: 243,197,153-248,437,482 , GRCh37 chr1: 243,360,455-248,600,783 ADSS2, HNRNPU, 124 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
    nsv7054066inversion1nstd229human GRCh38 chr1: 247,920,853-248,348,218 , GRCh37.p13 chr1: 248,084,155-248,511,520 OR2T33, OR2M1P, 23 more genes
    nsv7041671inversion1nstd229human GRCh38 chr1: 247,239,306-248,299,501 , GRCh37.p13 chr1: 247,402,608-248,462,803 OR9H1P, OR2L9P, 49 more genes
    nsv6677192copy number variation1nstd229human GRCh38 chr1: 247,898,206-248,021,800 , GRCh37.p13 chr1: 248,061,508-248,185,102 OR2L5, OR2L1P, 9 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
    nsv6668582copy number variation1nstd229human GRCh38 chr1: 247,987,039-248,360,199 , GRCh37.p13 chr1: 248,150,341-248,523,501 OR2M4, OR2M7, 17 more genes
    nsv6667121copy number variation1nstd229human GRCh38 chr1: 247,976,185-248,088,714 , GRCh37.p13 chr1: 248,139,487-248,252,016 OR2L3, OR2L1P, 6 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
    nsv6663848copy number variation1nstd229human GRCh38 chr1: 247,940,888-248,395,106 , GRCh37.p13 chr1: 248,104,190-248,558,407 OR14C36, OR2L13, 21 more genes
    nsv6660969copy number variation1nstd229human GRCh38 chr1: 247,944,356-248,045,011 , GRCh37.p13 chr1: 248,107,658-248,208,313 OR2L5, LOC105373275, 7 more genes
    nsv6659533copy number variation1nstd229human GRCh38 chr1: 247,373,080-248,325,181 , GRCh37.p13 chr1: 247,536,382-248,488,483 OR2L3, OR2L5, 47 more genes
    nsv6659249copy number variation1nstd229human GRCh38 chr1: 247,556,814-248,422,746 , GRCh37.p13 chr1: 247,720,116-248,586,047 OR2L13, TRIM58, 44 more genes
    nsv6658487copy number variation1nstd229human GRCh38 chr1: 247,988,601-248,057,100 , GRCh37.p13 chr1: 248,151,903-248,220,402 OR2L1P, OR2L6P, 4 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
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