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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv7039656inversion1nstd229human GRCh38 chr7: 75,704,904-77,508,509 , GRCh37.p13 chr7: 75,921,853-77,137,826 HSPB1, FAM185BP, 45 more genes
    nsv6836675copy number variation1nstd229human GRCh38 chr7: 77,317,982-77,449,580 , GRCh37.p13 chr7: 76,947,299-77,078,897 GSAP, LOC101927243
    nsv6835499copy number variation1nstd229human GRCh38 chr7: 77,345,101-77,620,000 , GRCh37.p13 chr7: 76,974,418-77,249,317 GCNT1P5, PTPN12, 2 more genes
    nsv6818709copy number variation1nstd229human GRCh38 chr7: 74,993,422-78,510,839 , GRCh37.p13 chr7: 75,921,853-78,140,156 TMEM120A, LOC105375359, 75 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6615708copy number variation1nstd223human GRCh38 chr7: 77,345,101-77,620,000 , GRCh37.p13 chr7: 76,974,418-77,249,317 GCNT1P5, LOC101927243, 2 more genes
    nsv6609612copy number variation1nstd223human GRCh38 chr7: 77,409,901-77,420,400 , GRCh37.p13 chr7: 77,039,218-77,049,717 LOC101927243, GSAP
    nsv6608583copy number variation1nstd223human GRCh38 chr7: 77,385,293-77,498,748 , GRCh37.p13 chr7: 77,014,610-77,128,065 GCNT1P5, GSAP, 1 more genes
    nsv6572498inversion1nstd223human GRCh38 chr7: 75,704,918-77,511,682 , GRCh37.p13 chr7: 75,921,853-77,140,999 LOC645324, FDPSP2, 45 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6291195copy number variation1nstd102humanUncertain significance GRCh37 chr7: 76,896,700-77,169,384 , GRCh38.p12 chr7: 77,267,383-77,540,067 LOC101927243, PTPN12, 4 more genes
    nsv6290688copy number variation1nstd102humanPathogenic GRCh38 chr7: 75,058,300-79,083,658 , GRCh37.p13 chr7: 75,921,853-78,712,974 GTF2IP1, TMEM60, 76 more genes
    nsv6137012copy number variation1nstd213human GRCh37 chr7: 76,580,000-78,000,001 , GRCh38.p12 chr7: 76,950,683-78,370,684 TMEM60, RPL13AP17, 25 more genes
    nsv6136262copy number variation1nstd213human GRCh37 chr7: 77,010,000-90,950,001 , GRCh38.p12 chr7: 77,380,683-91,320,686 , GRM3, 118 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv5692196mobile element insertion1nstd211human GRCh38 chr7: 77,418,359-77,418,359 , GRCh37.p13 chr7: 77,047,676-77,047,676 LOC101927243
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
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