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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5370378translocation1nstd200human GRCh38 chr9: 121,470,851-121,470,851 , GRCh38 chr7: 19,695,466-19,695,466 , GRCh37.p13 chr7: 19,735,089-19,735,089 , GRCh37.p13 chr9: 124,233,129-124,233,129 POLR1F, GGTA1
    nsv5353859translocation1nstd200human GRCh38 chr7: 19,709,023-19,709,023 , GRCh38 chr9: 121,470,864-121,470,864 , GRCh37.p13 chr9: 124,233,142-124,233,142 , GRCh37.p13 chr7: 19,748,646-19,748,646 POLR1F, GGTA1
    nsv5235037copy number variation1nstd204human GRCh38.p13 chr7: 19,705,585-19,733,299 , GRCh37.p13 chr7: 19,745,208-19,772,922 TMEM196, LOC107986774, 2 more genes
    nsv5230829copy number variation1nstd204human GRCh38.p13 chr7: 19,031,801-20,064,300 , GRCh37.p13 chr7: 19,071,424-20,103,923 LOC107986774, LOC107986773, 10 more genes
    nsv4955856copy number variation1nstd200human GRCh38 chr7: 19,701,396-19,703,814 , GRCh37.p13 chr7: 19,741,019-19,743,437 POLR1F, MIR3146
    nsv4953452copy number variation1nstd200human GRCh38 chr7: 19,223,736-19,975,909 , GRCh37.p13 chr7: 19,263,359-20,015,532 POLR1F, TMEM196, 7 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4826783copy number variation1nstd200human GRCh37 chr7: 19,741,019-19,743,437 , GRCh38.p12 chr7: 19,701,396-19,703,814 MIR3146, POLR1F
    nsv4768371copy number variation1nstd102humanPathogenic GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542 HDAC9, LOC101927668, 60 more genes
    nsv4674987copy number variation1nstd102humanPathogenic GRCh37 chr7: 13,886,653-20,267,202 , GRCh38.p12 chr7: 13,847,028-20,227,579 BZW2, LOC105375168, 64 more genes
    nsv4560404sequence alteration1nstd166human GRCh37.p13 chr7: 19,733,542-19,734,097 , GRCh38.p12 chr7: 19,693,919-19,694,474 POLR1F
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4139828copy number variation1nstd166human GRCh37.p13 chr7: 19,132,974-20,624,922 , GRCh38.p12 chr7: 19,093,351-20,585,299 LOC101927769, LOC105375181, 18 more genes
    nsv3922488copy number variation1nstd102humanPathogenic GRCh37 chr7: 16,161,141-20,647,522 , GRCh38 chr7: 16,121,516-20,607,899 , NCBI36 chr7: 16,127,666-20,614,047 HDAC9, LOC105375168, 53 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3920312copy number variation1nstd102humanUncertain significance GRCh38 chr7: 18,660,228-20,666,885 , NCBI36 chr7: 18,666,376-20,673,033 , GRCh37 chr7: 18,699,851-20,706,508 NPM1P13, LOC101927769, 24 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 MMD2, ICA1-AS1, 554 more genes
    nsv3917282copy number variation1nstd102humanPathogenic GRCh38 chr7: 19,145,712-22,193,713 , GRCh37 chr7: 19,185,335-22,233,331 , NCBI36 chr7: 19,151,860-22,199,856 MIR3146, RPS26P30, 33 more genes
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