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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713886mobile element insertion1nstd211human GRCh38 chr10: 70,407,127-70,407,127 , GRCh37.p13 chr10: 72,166,883-72,166,883 EIF4EBP2
    nsv5636156insertion1nstd207human GRCh38 chr10: 70,407,972-70,407,972 , GRCh37.p13 chr10: 72,167,728-72,167,728 EIF4EBP2
    nsv5557126sequence alteration1nstd206human GRCh38 chr10: 70,411,337-70,411,343 , GRCh37.p13 chr10: 72,171,093-72,171,099 EIF4EBP2
    nsv5536084insertion1nstd206human GRCh38 chr10: 70,411,337-70,411,337 , GRCh37.p13 chr10: 72,171,093-72,171,093 EIF4EBP2
    nsv5380872copy number variation2nstd102humanUncertain significance GRCh37 chr10: 72,179,670-72,360,658 , GRCh38.p12 chr10: 70,419,914-70,600,902 NODAL, EIF4EBP2, 3 more genes
    nsv5196984mobile element insertion1nstd203human GRCh38 chr10: 70,407,127-70,407,127 , GRCh37.p13 chr10: 72,166,883-72,166,883 EIF4EBP2
    nsv5122363mobile element insertion1nstd203human GRCh38 chr10: 70,418,280-70,418,284 , GRCh37.p13 chr10: 72,178,036-72,178,040 EIF4EBP2
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4757511insertion1nstd199human GRCh37 chr10: 72,167,660-72,167,660 , GRCh38.p12 chr10: 70,407,904-70,407,904 EIF4EBP2
    nsv4601421copy number variation1nstd183human GRCh37 chr10: 70,564,120-74,122,461 , GRCh38.p12 chr10: 68,804,363-72,362,703 , SGPL1, 79 more genes
    nsv4557203insertion1nstd166human GRCh37.p13 chr10: 72,166,391-72,166,391 , GRCh38.p12 chr10: 70,406,635-70,406,635 EIF4EBP2
    nsv4554971insertion1nstd166human GRCh37.p13 chr10: 72,166,400-72,166,400 , GRCh38.p12 chr10: 70,406,644-70,406,644 EIF4EBP2
    nsv4551085insertion1nstd166human GRCh37.p13 chr10: 72,166,299-72,166,299 , GRCh38.p12 chr10: 70,406,543-70,406,543 EIF4EBP2
    nsv4527226copy number variation1nstd166human GRCh37.p13 chr10: 72,132,999-72,496,000 , GRCh38.p12 chr10: 70,373,243-70,736,244 EIF4EBP2, NODAL, 6 more genes
    nsv4481170mobile element insertion1nstd166human GRCh37.p13 chr10: 72,168,272-72,168,272 , GRCh38.p12 chr10: 70,408,516-70,408,516 EIF4EBP2
    nsv4480182mobile element insertion1nstd166human GRCh37.p13 chr10: 72,166,421-72,166,421 , GRCh38.p12 chr10: 70,406,665-70,406,665 EIF4EBP2
    nsv4441389insertion1nstd175human GRCh37 chr10: 72,167,700-72,167,700 , GRCh38.p12 chr10: 70,407,944-70,407,944 EIF4EBP2
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4190112copy number variation1nstd166human GRCh37.p13 chr10: 72,183,179-72,187,964 , GRCh38.p12 chr10: 70,423,423-70,428,208 EIF4EBP2
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