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Items: 1 to 20 of 996

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7147992copy number variation1nstd232human GRCh37.p13 chr8: 1,236,830-1,237,052 , GRCh38.p12 chr8: 1,287,441-1,287,665 DLGAP2
    nsv7147877copy number variation1nstd232human GRCh37.p13 chr8: 1,324,820-1,324,883 , GRCh38.p12 chr8: 1,376,654-1,376,717 DLGAP2
    nsv7147763copy number variation1nstd232human GRCh37.p13 chr8: 1,597,435-1,597,485 , GRCh38.p12 chr8: 1,649,269-1,649,319 , GRCh38.p12 chr8|NT_187654.1: 258,652-258,702 DLGAP2
    nsv7147491copy number variation1nstd232human GRCh37.p13 chr8: 1,040,314-1,040,379 , GRCh38.p12 chr8: 1,090,314-1,090,379 , GRCh38.p12 chr8|NT_187568.1: 231,604-231,669 DLGAP2
    nsv7147476copy number variation1nstd232human GRCh37.p13 chr8: 927,750-927,886 , GRCh38.p12 chr8: 977,750-977,886 , GRCh38.p12 chr8|NT_187568.1: 116,110-116,246 DLGAP2
    nsv7147348copy number variation1nstd232human GRCh37.p13 chr8: 1,045,058-1,045,113 , GRCh38.p12 chr8: 1,095,058-1,095,113 , GRCh38.p12 chr8|NT_187568.1: 236,348-236,403 DLGAP2
    nsv7147084copy number variation1nstd232human GRCh37.p13 chr8: 1,456,482-1,456,556 , GRCh38.p12 chr8: 1,508,316-1,508,390 , GRCh38.p12 chr8|NT_187565.1: 213,848-213,922 DLGAP2
    nsv7146946copy number variation1nstd232human GRCh37.p13 chr8: 1,407,375-1,407,447 , GRCh38.p12 chr8: 1,459,209-1,459,281 , GRCh38.p12 chr8|NT_187565.1: 164,741-164,813 , GRCh38.p12 chr8|NT_187654.1: 69,562-69,634 DLGAP2
    nsv7146538copy number variation1nstd232human GRCh37.p13 chr8: 1,469,338-1,469,453 , GRCh38.p12 chr8|NT_187565.1: 226,704-226,819 , GRCh38.p12 chr8|NT_187654.1: 132,474-132,531 , GRCh38.p12 chr8: 1,521,172-1,521,287 DLGAP2
    nsv7146431insertion1nstd232human GRCh37.p13 chr8: 1,286,974-1,286,974 , GRCh38.p12 chr8: 1,338,808-1,338,808 , GRCh38.p12 chr8|NT_187565.1: 58,024-58,024 DLGAP2
    nsv7146223insertion1nstd232human GRCh37.p13 chr8: 1,574,144-1,574,144 , GRCh38.p12 chr8: 1,625,978-1,625,978 , GRCh38.p12 chr8|NT_187654.1: 235,998-235,998 , GRCh38.p12 chr8|NT_187680.1: 39,364-39,364 DLGAP2
    nsv7146118copy number variation1nstd232human GRCh37.p13 chr8: 1,328,000-1,328,049 , GRCh38.p12 chr8: 1,379,834-1,379,883 , GRCh38.p12 chr8|NT_187565.1: 98,716-98,765 DLGAP2
    nsv7145900copy number variation1nstd232human GRCh37.p13 chr8: 940,354-940,407 , GRCh38.p12 chr8: 990,354-990,407 , GRCh38.p12 chr8|NT_187568.1: 131,635-131,688 DLGAP2
    nsv7145783copy number variation1nstd232human GRCh37.p13 chr8: 1,265,079-1,265,148 , GRCh38.p12 chr8: 1,316,913-1,316,982 , GRCh38.p12 chr8|NT_187565.1: 36,129-36,198 DLGAP2
    nsv7145695copy number variation1nstd232human GRCh37.p13 chr8: 709,059-709,139 , GRCh38.p12 chr8: 759,059-759,139 , GRCh38.p12 chr8|NT_187572.1: 40,650-40,730 DLGAP2
    nsv7145325insertion1nstd232human GRCh37.p13 chr8: 940,364-940,364 , GRCh38.p12 chr8: 990,364-990,364 , GRCh38.p12 chr8|NT_187568.1: 131,645-131,645 DLGAP2
    nsv7145198copy number variation1nstd232human GRCh37.p13 chr8: 1,071,684-1,071,745 , GRCh38.p12 chr8: 1,121,684-1,121,745 , GRCh38.p12 chr8|NT_187568.1: 262,974-263,035 DLGAP2
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