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Items: 1 to 20 of 543

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117673copy number variation1nstd186human GRCh37 chr6: 31,948,777-32,013,177 , GRCh38.p12 chr6: 31,981,000-32,045,400 C4A, C4B, 6 more genes
    nsv5901961copy number variation1nstd209human GRCh38 chr6: 32,060,300-32,060,367 , GRCh37.p13 chr6: 32,028,077-32,028,144 TNXB
    nsv5887714copy number variation1nstd209human GRCh38 chr6: 32,058,184-32,061,607 , GRCh37.p13 chr6: 32,025,961-32,029,384 TNXB
    nsv5845235copy number variation3nstd209human GRCh38 chr6: 32,037,219-32,040,784 , GRCh37.p13 chr6: 32,004,996-32,008,561 TNXB, CYP21A2
    nsv5845136copy number variation1nstd209human GRCh38 chr6: 32,058,118-32,061,541 , GRCh37.p13 chr6: 32,025,895-32,029,318 TNXB
    nsv5844612copy number variation2nstd209human GRCh38 chr6: 32,050,753-32,054,012 , GRCh37.p13 chr6: 32,018,530-32,021,789 TNXB
    nsv5844611copy number variation3nstd209human GRCh38 chr6: 32,036,849-32,040,410 , GRCh37.p13 chr6: 32,004,626-32,008,187 CYP21A2, TNXB
    nsv5693273mobile element insertion1nstd211human GRCh38 chr6: 32,099,912-32,099,912 , GRCh37.p13 chr6: 32,067,689-32,067,689 TNXB
    nsv5633731insertion1nstd207human GRCh38 chr6: 32,060,300-32,060,300 , GRCh37.p13 chr6: 32,028,077-32,028,077 TNXB
    nsv5632416insertion1nstd207human GRCh38 chr6: 32,043,718-32,043,718 , GRCh37.p13 chr6: 32,011,495-32,011,495 TNXB
    nsv5579368copy number variation1nstd207human GRCh38 chr6: 32,039,907-32,039,974 , GRCh37.p13 chr6: 32,007,684-32,007,751 TNXB, CYP21A2
    nsv5472828copy number variation1nstd206human GRCh38 chr6: 32,053,585-32,056,783 , GRCh37.p13 chr6: 32,021,362-32,024,560 TNXB
    nsv5460556copy number variation1nstd206human GRCh38 chr6: 32,083,063-32,083,204 , GRCh37.p13 chr6: 32,050,840-32,050,981 TNXB
    nsv5456987copy number variation1nstd206human GRCh38 chr6: 32,056,027-32,061,608 , GRCh37.p13 chr6: 32,023,804-32,029,385 TNXB
    nsv5456914copy number variation1nstd206human GRCh38 chr6: 32,039,903-32,039,975 , GRCh37.p13 chr6: 32,007,680-32,007,752 TNXB, CYP21A2
    nsv5418497copy number variation1nstd206human GRCh38 chr6: 31,981,000-32,045,400 , GRCh37.p13 chr6: 31,948,777-32,013,177 C4A, C4B, 6 more genes
    nsv5388756copy number variation1nstd186human GRCh37 chr6: 32,026,012-32,029,314 , GRCh38.p12 chr6: 32,058,235-32,061,537 TNXB
    nsv5387082copy number variation1nstd186human GRCh37 chr6: 32,026,012-32,029,358 , GRCh38.p12 chr6: 32,058,235-32,061,581 TNXB
    nsv5378355translocation1nstd200human GRCh38 chr6: 32,072,015-32,072,015 , GRCh38 chr6: 32,084,890-32,084,890 , GRCh37.p13 chr6: 32,052,667-32,052,667 , GRCh37.p13 chr6: 32,039,792-32,039,792 TNXB
    nsv5315990copy number variation1nstd204human GRCh38.p13 chr6: 32,057,823-32,061,946 , GRCh37.p13 chr6: 32,025,600-32,029,723 TNXB
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