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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050314inversion1nstd229human GRCh37.p13 chr7|NW_004775430.1: 47,349-274,521 , GRCh38 chr7: 65,594,518-65,831,150 , GRCh37.p13 chr7: 65,059,431-65,286,677 LINC03006, CCT6P1, 6 more genes
    nsv7041397inversion1nstd229human GRCh38 chr7: 65,600,026-71,276,703 , GRCh37.p13 chr7: 65,286,678-70,741,689 GALNT17, MTCO1P25, 74 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
    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
    nsv6305485copy number variation1nstd186human GRCh37 chr7: 65,052,394-65,286,677 , GRCh38.p12 chr7: 65,587,481-65,821,690 LOC402279, LINC03006, 6 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
    nsv6010707copy number variation1nstd212human GRCh37.p13 chr7|NW_004775430.1: 202,156-212,137 , GRCh38 chr7: 65,749,325-65,759,306 , GRCh37.p13 chr7: 65,214,312-65,224,293 LINC03006, CCT6P1, 2 more genes
    nsv5922394copy number variation1nstd209human GRCh38 chr7: 65,103,162-65,765,400 , GRCh37.p13 chr7: 64,563,540-65,012,082 , CCT6P1, 13 more genes
    nsv5920709copy number variation1nstd209human GRCh38 chr7: 65,106,549-65,795,958 , GRCh37.p13 chr7: 64,566,927-65,012,082 , LOC402279, 14 more genes
    nsv5907866copy number variation1nstd209human GRCh38 chr7: 65,084,132-65,773,545 , GRCh37.p13 chr7: 64,544,510-65,012,082 , LOC101929322, 15 more genes
    nsv5847110copy number variation1nstd209human GRCh37.p13 chr7|NW_004775430.1: 190,118-212,738 , GRCh38 chr7: 65,737,287-65,759,907 , GRCh37.p13 chr7: 65,202,279-65,224,894 LINC03006, CCT6P1, 2 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
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