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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    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
    nsv7065650inversion1nstd229human GRCh38 chr8: 38,105,502-38,105,581 , GRCh37.p13 chr8: 37,963,020-37,963,099 ASH2L
    nsv6852374copy number variation1nstd229human GRCh38 chr8: 38,121,696-38,125,236 , GRCh37.p13 chr8: 37,979,214-37,982,754 RNU6-988P, ASH2L
    nsv6851770copy number variation1nstd229human GRCh38 chr8: 38,117,011-38,118,402 , GRCh37.p13 chr8: 37,974,529-37,975,920 ASH2L
    nsv6846152copy number variation1nstd229human GRCh38 chr8: 38,083,243-38,110,051 , GRCh37.p13 chr8: 37,940,761-37,967,569 ASH2L
    nsv6839349copy number variation1nstd229human GRCh38 chr8: 38,140,425-38,140,710 , GRCh37.p13 chr8: 37,997,943-37,998,228 STAR, ASH2L
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6557794inversion1nstd223human GRCh38 chr8: 38,123,920-38,125,582 , GRCh37.p13 chr8: 37,981,438-37,983,100 ASH2L
    nsv6557388inversion1nstd223human GRCh38 chr8: 38,140,332-38,140,709 , GRCh37.p13 chr8: 37,997,850-37,998,227 STAR, ASH2L
    nsv6430795copy number variation1nstd223human GRCh38 chr8: 38,116,164-38,119,835 , GRCh37.p13 chr8: 37,973,682-37,977,353 ASH2L
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv6137281copy number variation1nstd213human GRCh37 chr8: 37,350,000-38,410,001 , GRCh38.p12 chr8: 37,492,482-38,552,483 ADRB3, EIF4EBP1, 32 more genes
    nsv6136673copy number variation1nstd213human GRCh37 chr8: 37,880,000-38,230,001 , GRCh38.p12 chr8: 38,022,482-38,372,483 STAR, ASH2L, 9 more genes
    nsv6017812copy number variation1nstd212human GRCh38 chr8: 38,140,230-38,140,305 , GRCh37.p13 chr8: 37,997,748-37,997,823 ASH2L
    nsv6002090copy number variation1nstd212human GRCh38 chr8: 38,105,104-38,158,349 , GRCh37.p13 chr8: 37,962,622-38,015,867 STAR, ASH2L, 2 more genes
    nsv5711071mobile element insertion1nstd211human GRCh38 chr8: 38,114,772-38,114,772 , GRCh37.p13 chr8: 37,972,290-37,972,290 ASH2L
    nsv5490999copy number variation1nstd206human GRCh38 chr8: 38,138,320-38,138,385 , GRCh37.p13 chr8: 37,995,838-37,995,903 ASH2L
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