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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv7095681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008 SLC35A3, S1PR1-DT, 29 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6657975copy number variation1nstd229human GRCh38 chr1: 99,498,947-100,487,486 , GRCh37.p13 chr1: 99,964,503-100,953,042 CDC14A, AGL, 21 more genes
    nsv6638249copy number variation1nstd229human GRCh38 chr1: 100,279,384-100,286,367 , GRCh37.p13 chr1: 100,744,940-100,751,923 RTCA, MIR553
    nsv6543998inversion1nstd223human GRCh38 chr1: 100,270,811-100,271,295 , GRCh37.p13 chr1: 100,736,367-100,736,851 RTCA
    nsv6536283inversion1nstd223human GRCh38 chr1: 100,280,831-100,281,723 , GRCh37.p13 chr1: 100,746,387-100,747,279 MIR553, RTCA
    nsv6327216copy number variation1nstd223human GRCh38 chr1: 100,289,122-100,289,808 , GRCh37.p13 chr1: 100,754,678-100,755,364 RTCA
    nsv6323410copy number variation1nstd223human GRCh38 chr1: 100,256,389-100,301,437 , GRCh37.p13 chr1: 100,721,945-100,766,993 RTCA, RTCA-AS1, 1 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6290366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608 LOC105379827, RPSAP19, 63 more genes
    nsv6133669copy number variation1nstd213human GRCh37 chr1: 95,900,000-101,030,001 , GRCh38.p12 chr1: 95,434,444-100,564,445 PALMD, LRRC39, 56 more genes
    nsv5724944mobile element insertion2nstd211human GRCh38 chr1: 100,270,189-100,270,189 , GRCh37.p13 chr1: 100,735,745-100,735,745 RTCA
    nsv5684203mobile element insertion1nstd211human GRCh38 chr1: 100,273,212-100,273,212 , GRCh37.p13 chr1: 100,738,768-100,738,768 RTCA
    nsv5683686mobile element insertion1nstd211human GRCh38 chr1: 100,283,956-100,283,956 , GRCh37.p13 chr1: 100,749,512-100,749,512 RTCA
    nsv5425265copy number variation1nstd206human GRCh38 chr1: 100,283,406-100,284,572 , GRCh37.p13 chr1: 100,748,962-100,750,128 RTCA
    nsv5408777mobile element insertion1nstd206human GRCh38 chr1: 100,273,212-100,273,263 , GRCh37.p13 chr1: 100,738,768-100,738,819 RTCA
    nsv5353656translocation1nstd200human GRCh38 chr1: 100,289,118-100,289,118 , GRCh38 chr1: 100,289,808-100,289,808 , GRCh37.p13 chr1: 100,754,674-100,754,674 , GRCh37.p13 chr1: 100,755,364-100,755,364 RTCA
    nsv5291352copy number variation1nstd204human GRCh38.p13 chr1: 100,289,108-100,289,811 , GRCh37.p13 chr1: 100,754,664-100,755,367 RTCA
    nsv4906383copy number variation1nstd200human GRCh38 chr1: 100,283,455-100,284,523 , GRCh37.p13 chr1: 100,749,011-100,750,079 RTCA
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