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Items: 1 to 20 of 494

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7097662copy number variation2nstd102humanUncertain significance GRCh37 chr8: 41,518,984-43,054,712 , GRCh38.p12 chr8: 41,661,466-43,199,569 LOC101059972, IKBKB-DT, 31 more genes
    nsv7065906inversion1nstd229human GRCh38 chr8: 43,022,562-43,025,833 , GRCh37.p13 chr8: 42,877,705-42,880,976 HOOK3
    nsv6857833copy number variation1nstd229human GRCh38 chr8: 42,930,797-42,941,785 , GRCh37.p13 chr8: 42,785,940-42,796,928 HOOK3
    nsv6856886copy number variation1nstd229human GRCh38 chr8: 43,025,389-43,061,026 , GRCh37.p13 chr8: 42,880,532-42,916,169 HOOK3, FNTA
    nsv6855651copy number variation1nstd229human GRCh38 chr8: 42,989,149-42,993,640 , GRCh37.p13 chr8: 42,844,292-42,848,783 HOOK3
    nsv6850363copy number variation1nstd229human GRCh38 chr8: 42,921,675-42,922,029 , GRCh37.p13 chr8: 42,776,818-42,777,172 HOOK3
    nsv6848943copy number variation1nstd229human GRCh38 chr8: 42,933,489-42,938,133 , GRCh37.p13 chr8: 42,788,632-42,793,276 HOOK3
    nsv6847812copy number variation1nstd229human GRCh38 chr8: 42,988,633-42,988,670 , GRCh37.p13 chr8: 42,843,776-42,843,813 HOOK3
    nsv6844627copy number variation1nstd229human GRCh38 chr8: 42,979,549-42,979,605 , GRCh37.p13 chr8: 42,834,692-42,834,748 HOOK3
    nsv6842239copy number variation1nstd229human GRCh38 chr8: 42,891,987-42,896,477 , GRCh37.p13 chr8: 42,747,130-42,751,620 RNF170, MIR4469, 1 more genes
    nsv6841466copy number variation1nstd229human GRCh38 chr8: 42,948,633-43,067,501 , GRCh37.p13 chr8: 42,803,776-42,922,644 HOOK3, FNTA
    nsv6839543copy number variation1nstd229human GRCh38 chr8: 42,998,404-43,001,014 , GRCh37.p13 chr8: 42,853,547-42,856,157 HOOK3
    nsv6637131copy number variation1nstd102humanPathogenic GRCh37 chr8: 42,303,398-43,002,481 , GRCh38.p12 chr8: 42,445,880-43,147,338 RNU1-124P, LOC105379396, 13 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6575412inversion1nstd223human GRCh38 chr8: 43,014,254-43,014,475 , GRCh37.p13 chr8: 42,869,397-42,869,618 HOOK3
    nsv6573816inversion1nstd223human GRCh38 chr8: 42,991,415-42,992,632 , GRCh37.p13 chr8: 42,846,558-42,847,775 HOOK3
    nsv6573597inversion1nstd223human GRCh38 chr8: 43,015,088-43,015,794 , GRCh37.p13 chr8: 42,870,231-42,870,937 HOOK3
    nsv6570328inversion1nstd223human GRCh38 chr8: 43,020,653-43,021,408 , GRCh37.p13 chr8: 42,875,796-42,876,551 HOOK3
    nsv6570039inversion1nstd223human GRCh38 chr8: 43,011,633-43,012,856 , GRCh37.p13 chr8: 42,866,776-42,867,999 HOOK3
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