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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5867874copy number variation1nstd209human GRCh38 chr1: 77,879,455-77,880,101 , GRCh37.p13 chr1: 78,345,140-78,345,786 MIGA1, NEXN-AS1
    nsv5690293mobile element insertion1nstd211human GRCh38 chr1: 77,887,983-77,887,983 , GRCh37.p13 chr1: 78,353,668-78,353,668 NEXN-AS1, NEXN
    nsv5614275insertion1nstd207human GRCh38 chr1: 77,887,947-77,887,947 , GRCh37.p13 chr1: 78,353,632-78,353,632 NEXN-AS1, NEXN
    nsv5575627copy number variation1nstd207human GRCh38 chr1: 77,887,912-77,887,962 , GRCh37.p13 chr1: 78,353,597-78,353,647 NEXN, NEXN-AS1
    nsv5416018copy number variation1nstd206human GRCh38 chr1: 77,887,204-77,887,503 , GRCh37.p13 chr1: 78,352,889-78,353,188 NEXN, NEXN-AS1
    nsv5189086mobile element insertion1nstd203human GRCh38 chr1: 77,880,039-77,880,053 , GRCh37.p13 chr1: 78,345,724-78,345,738 NEXN-AS1, MIGA1
    nsv4903670copy number variation1nstd200human GRCh38 chr1: 77,866,141-77,949,695 , GRCh37.p13 chr1: 78,331,826-78,415,380 MIGA1, NEXN-AS1, 2 more genes
    nsv4896499copy number variation1nstd200human GRCh38 chr1: 77,888,906-77,888,978 , GRCh37.p13 chr1: 78,354,591-78,354,663 NEXN, NEXN-AS1
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783875copy number variation1nstd200human GRCh37 chr1: 78,345,145-78,345,787 , GRCh38.p12 chr1: 77,879,460-77,880,102 NEXN-AS1, MIGA1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4754164insertion1nstd199human GRCh37 chr1: 78,353,620-78,353,620 , GRCh38.p12 chr1: 77,887,935-77,887,935 NEXN, NEXN-AS1
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4724281insertion1nstd186human GRCh37 chr1: 78,353,638-78,353,638 , GRCh38.p12 chr1: 77,887,953-77,887,953 NEXN, NEXN-AS1
    nsv4680287copy number variation1nstd189human GRCh37.p13 chr1: 77,366,676-80,161,301 , GRCh38.p12 chr1: 76,900,991-79,695,616 PTGFR, FUBP1, 42 more genes
    nsv4674427copy number variation1nstd102humanUncertain significance GRCh37 chr1: 78,257,937-79,159,519 , GRCh38.p12 chr1: 77,792,252-78,693,834 LOC100131495, RNA5SP22, 19 more genes
    nsv4535012insertion1nstd166human GRCh37.p13 chr1: 78,353,638-78,353,638 , GRCh38.p12 chr1: 77,887,953-77,887,953 NEXN, NEXN-AS1
    nsv4462094mobile element insertion1nstd166human GRCh37.p13 chr1: 78,354,930-78,354,930 , GRCh38.p12 chr1: 77,889,245-77,889,245 NEXN-AS1, NEXN
    nsv4454000copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657 NEXN, LOC107985391, 209 more genes
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