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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096008copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,304,994-12,569,078 , GRCh38.p12 chr1: 9,244,935-12,509,024 NMNAT1, DISP3, 91 more genes
    nsv7095685copy number variation1nstd102humanPathogenic GRCh37 chr1: 10,041,069-10,042,759 , GRCh38.p12 chr1: 9,981,011-9,982,701 NMNAT1
    nsv7095682copy number variation1nstd102humanPathogenic GRCh37 chr1: 10,032,132-10,032,266 , GRCh38.p12 chr1: 9,972,074-9,972,208 NMNAT1
    nsv7095679copy number variation1nstd102humanPathogenic GRCh37 chr1: 10,027,411-10,045,246 , GRCh38.p12 chr1: 9,967,353-9,985,188 NMNAT1, MIR5697
    nsv7095543copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,770,514-11,264,780 , GRCh38.p12 chr1: 9,710,456-11,204,723 DFFA, ANGPTL7, 38 more genes
    nsv7095302copy number variation1nstd102humanPathogenic GRCh37 chr1: 10,032,132-10,035,853 , GRCh38.p12 chr1: 9,972,074-9,975,795 NMNAT1
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7048193inversion1nstd229human GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883 PRAMEF36P, HNRNPCL3, 193 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv6658085copy number variation1nstd229human GRCh38 chr1: 9,990,756-9,996,450 , GRCh37.p13 chr1: 10,050,814-10,056,508 RBP7, NMNAT1
    nsv6658076copy number variation1nstd229human GRCh38 chr1: 9,953,267-9,962,970 , GRCh37.p13 chr1: 10,013,325-10,023,028 NMNAT1, TMEM274P
    nsv6658060copy number variation1nstd229human GRCh38 chr1: 9,989,602-9,992,537 , GRCh37.p13 chr1: 10,049,660-10,052,595 NMNAT1
    nsv6658046copy number variation1nstd229human GRCh38 chr1: 9,901,485-10,062,847 , GRCh37.p13 chr1: 9,961,543-10,122,905 TMEM274P, RN7SKP269, 8 more genes
    nsv6657983copy number variation1nstd229human GRCh38 chr1: 9,978,112-9,978,246 , GRCh37.p13 chr1: 10,038,170-10,038,304 NMNAT1
    nsv6657919copy number variation1nstd229human GRCh38 chr1: 9,803,781-10,372,657 , GRCh37.p13 chr1: 9,863,839-10,432,715 RN7SL731P, MIR5697, 14 more genes
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