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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041397inversion1nstd229human GRCh38 chr7: 65,600,026-71,276,703 , GRCh37.p13 chr7: 65,286,678-70,741,689 GALNT17, MTCO1P25, 74 more genes
    nsv6835608copy number variation1nstd229human GRCh38 chr7: 65,825,345-66,840,559 , GRCh37.p13 chr7: 65,290,332-66,305,546 LOC346329, RABGEF1P1, 27 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
    nsv6631986copy number variation1nstd224human GRCh37 chr7: 65,202,326-65,326,821 , GRCh38.p12 chr7: 65,737,334-65,861,834 LOC84214, LINC03006, 6 more genes
    nsv6619355copy number variation1nstd223human GRCh38 chr7: 65,035,202-65,870,265 , GRCh37.p13 chr7: 64,495,580-65,335,252 CCT6P1, RNU6-912P, 23 more genes
    nsv6611499copy number variation1nstd223human GRCh38 chr7: 65,664,001-65,910,200 , GRCh37.p13 chr7|NW_004775430.1: 116,832-274,521 , GRCh37.p13 chr7: 65,128,948-65,286,677 RNU6-973P, RNU6-912P, 8 more genes
    nsv6611470copy number variation1nstd223human GRCh38 chr7: 65,838,954-65,839,670 , GRCh37.p13 chr7: 65,303,941-65,304,657 LOC84214
    nsv6609669copy number variation1nstd223human GRCh38 chr7: 65,587,481-65,879,642 , GRCh37.p13 chr7: 65,052,394-65,286,677 , GRCh37.p13 chr7|NW_004775430.1: 40,312-274,521 INTS4P2, GTF2IP5, 9 more genes
    nsv6608610copy number variation1nstd223human GRCh38 chr7: 65,035,155-65,869,998 , GRCh37.p13 chr7: 64,495,533-65,334,985 CLUHP7, LOC105375334, 23 more genes
    nsv6606714copy number variation1nstd223human GRCh38 chr7: 65,038,637-65,873,563 , GRCh37.p13 chr7: 64,499,015-65,338,550 RSL24D1P3, LOC100533634, 23 more genes
    nsv6601679copy number variation1nstd223human GRCh38 chr7: 65,055,051-65,888,939 , GRCh37.p13 chr7: 64,515,429-65,353,926 RNU6-912P, LOC84214, 21 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6291136copy number variation1nstd102humanUncertain significance GRCh37 chr7: 64,651,626-66,010,636 , GRCh38.p12 chr7: 65,191,248-66,545,649 SNORA22, LOC105375334, 35 more genes
    nsv6135777copy number variation1nstd213human GRCh37 chr7: 65,150,000-70,530,001 , GRCh38.p12 chr7: 65,685,031-71,065,015 ASL, GUSB, 72 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486433copy number variation1nstd206human GRCh38 chr7: 65,840,996-65,841,190 , GRCh37.p13 chr7: 65,305,983-65,306,177 LOC84214
    nsv5476182copy number variation1nstd206human GRCh38 chr7: 65,587,481-65,879,647 , GRCh37.p13 chr7: 65,052,394-65,286,677 , GRCh37.p13 chr7|NW_004775430.1: 40,312-274,521 GTF2IP5, SNORA22, 9 more genes
    nsv5300566copy number variation1nstd204human GRCh38.p13 chr7: 65,587,471-65,879,656 , GRCh37.p13 chr7: 65,052,384-65,286,686 , GRCh37.p13 chr7|NW_004775430.1: 40,302-274,530 VKORC1L1, CCT6P1, 9 more genes
    nsv5238646copy number variation1nstd204human GRCh38.p13 chr7: 65,835,901-65,879,700 , GRCh37.p13 chr7: 65,300,888-65,344,687 LOC84214, VKORC1L1, 1 more genes
    nsv5237482copy number variation1nstd204human GRCh38.p13 chr7: 65,690,901-66,099,000 , GRCh37.p13 chr7: 65,286,678-65,563,987 LOC84214, LOC105375336, 14 more genes
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