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Items: 1 to 20 of 528

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096008copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,304,994-12,569,078 , GRCh38.p12 chr1: 9,244,935-12,509,024 NMNAT1, DISP3, 91 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv7039436inversion1nstd229human GRCh38 chr1: 9,354,470-9,524,241 , GRCh37.p13 chr1: 9,414,529-9,584,300 SPSB1, LINC02606, 1 more genes
    nsv6657543copy number variation1nstd229human GRCh38 chr1: 9,362,122-9,365,462 , GRCh37.p13 chr1: 9,422,181-9,425,521 SPSB1
    nsv6657534copy number variation1nstd229human GRCh38 chr1: 9,332,075-9,332,106 , GRCh37.p13 chr1: 9,392,134-9,392,165 SPSB1
    nsv6657374copy number variation1nstd229human GRCh38 chr1: 9,335,202-9,335,498 , GRCh37.p13 chr1: 9,395,261-9,395,557 SPSB1
    nsv6657369copy number variation1nstd229human GRCh38 chr1: 9,328,013-9,331,378 , GRCh37.p13 chr1: 9,388,072-9,391,437 SPSB1
    nsv6657352copy number variation1nstd229human GRCh38 chr1: 9,300,895-9,303,509 , GRCh37.p13 chr1: 9,360,954-9,363,568 SPSB1
    nsv6657177copy number variation1nstd229human GRCh38 chr1: 9,221,022-9,296,863 , GRCh37.p13 chr1: 9,281,081-9,356,922 H6PD, SPSB1
    nsv6657116copy number variation1nstd229human GRCh38 chr1: 9,245,538-9,312,734 , GRCh37.p13 chr1: 9,305,597-9,372,793 H6PD, SPSB1
    nsv6657044copy number variation1nstd229human GRCh38 chr1: 9,097,701-11,036,600 , GRCh37.p13 chr1: 9,157,760-11,096,657 CENPS-CORT, H6PD, 46 more genes
    nsv6656653copy number variation1nstd229human GRCh38 chr1: 9,337,828-9,337,995 , GRCh37.p13 chr1: 9,397,887-9,398,054 SPSB1
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