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Items: 1 to 20 of 296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918784copy number variation1nstd209human GRCh38 chr7: 17,301,592-17,302,697 , GRCh37.p13 chr7: 17,341,216-17,342,321 AHR
    nsv5845910copy number variation2nstd209human GRCh38 chr7: 17,301,205-17,302,804 , GRCh37.p13 chr7: 17,340,829-17,342,428 AHR
    nsv5723466mobile element insertion1nstd211human GRCh38 chr7: 17,324,843-17,324,843 , GRCh37.p13 chr7: 17,364,467-17,364,467 AHR
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5471306copy number variation1nstd206human GRCh38 chr7: 16,875,809-17,377,161 , GRCh37.p13 chr7: 16,915,433-17,416,785 AHR, AGR3, 7 more genes
    nsv5468287copy number variation1nstd206human GRCh38 chr7: 17,287,896-17,297,740 , GRCh37.p13 chr7: 17,327,520-17,337,364 LOC101927609, AHR
    nsv5458995copy number variation1nstd206human GRCh38 chr7: 17,317,890-17,318,036 , GRCh37.p13 chr7: 17,357,514-17,357,660 AHR
    nsv5317634copy number variation1nstd204human GRCh38.p13 chr7: 16,080,765-17,645,128 , GRCh37.p13 chr7: 16,120,390-17,684,752 AHR, RAD17P1, 23 more genes
    nsv5237229copy number variation1nstd204human GRCh38.p13 chr7: 17,291,138-17,311,983 , GRCh37.p13 chr7: 17,330,762-17,351,607 AHR, LOC101927609
    nsv5223578copy number variation1nstd204human GRCh38.p13 chr7: 16,522,001-17,645,100 , GRCh37.p13 chr7: 16,561,626-17,684,724 LOC105375172, LOC105375169, 18 more genes
    nsv5221872copy number variation1nstd204human GRCh38.p13 chr7: 17,307,003-17,309,683 , GRCh37.p13 chr7: 17,346,627-17,349,307 AHR
    nsv4955767copy number variation1nstd200human GRCh38 chr7: 17,320,299-17,326,309 , GRCh37.p13 chr7: 17,359,923-17,365,933 AHR
    nsv4953440copy number variation1nstd200human GRCh38 chr7: 17,346,507-17,590,172 , GRCh37.p13 chr7: 17,386,131-17,629,796 LOC105375172, LINC02889, 3 more genes
    nsv4953439copy number variation1nstd200human GRCh38 chr7: 17,258,600-17,298,993 , GRCh37.p13 chr7: 17,298,224-17,338,617 AHR, LOC101927609
    nsv4953435copy number variation1nstd200human GRCh38 chr7: 17,135,121-17,642,878 , GRCh37.p13 chr7: 17,174,745-17,682,502 AHR, LOC101927609, 5 more genes
    nsv4953427copy number variation1nstd200human GRCh38 chr7: 16,875,809-17,377,161 , GRCh37.p13 chr7: 16,915,433-17,416,785 LOC107986772, AGR3, 7 more genes
    nsv4953420copy number variation1nstd200human GRCh38 chr7: 16,080,775-17,645,126 , GRCh37.p13 chr7: 16,120,400-17,684,750 LOC107986772, TSPAN13, 23 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4828774copy number variation1nstd200human GRCh37 chr7: 17,090,823-17,758,241 , GRCh38.p12 chr7: 17,051,199-17,718,617 LOC107986772, LOC105375171, 5 more genes
    nsv4828771copy number variation1nstd200human GRCh37 chr7: 16,915,430-17,416,788 , GRCh38.p12 chr7: 16,875,806-17,377,164 AHR, LOC105375170, 7 more genes
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