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Items: 1 to 20 of 507

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057332inversion1nstd229human GRCh38 chr4: 152,510,340-152,517,336 , GRCh37.p13 chr4: 153,431,492-153,438,488 FBXW7
    nsv7055634inversion1nstd229human GRCh38 chr4: 152,515,897-153,221,494 , GRCh37.p13 chr4: 153,437,049-154,142,646 MIR4453, NSA2P6, 12 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv7046905inversion1nstd229human GRCh38 chr4: 151,269,540-154,434,057 , GRCh37.p13 chr4: 152,190,692-155,355,209 GATB, LOC105377492, 47 more genes
    nsv7042689inversion1nstd229human GRCh38 chr4: 152,435,195-152,435,252 , GRCh37.p13 chr4: 153,356,347-153,356,404 FBXW7
    nsv6757976copy number variation1nstd229human GRCh38 chr4: 152,332,901-152,336,800 , GRCh37.p13 chr4: 153,254,053-153,257,952 FBXW7, FBXW7-AS1
    nsv6757023copy number variation1nstd229human GRCh38 chr4: 152,401,901-152,518,700 , GRCh37.p13 chr4: 153,323,053-153,439,852 MIR3140, FBXW7
    nsv6756598copy number variation1nstd229human GRCh38 chr4: 152,493,101-152,847,600 , GRCh37.p13 chr4: 153,414,253-153,768,752 TMEM154, TIGD4, 8 more genes
    nsv6755685copy number variation1nstd229human GRCh38 chr4: 152,442,701-152,859,600 , GRCh37.p13 chr4: 153,363,853-153,780,752 ARFIP1, FBXW7, 9 more genes
    nsv6754493copy number variation1nstd229human GRCh38 chr4: 152,395,038-152,395,187 , GRCh37.p13 chr4: 153,316,190-153,316,339 FBXW7
    nsv6753214copy number variation1nstd229human GRCh38 chr4: 152,426,864-152,432,022 , GRCh37.p13 chr4: 153,348,016-153,353,174 FBXW7
    nsv6753178copy number variation1nstd229human GRCh38 chr4: 152,363,675-152,400,662 , GRCh37.p13 chr4: 153,284,827-153,321,814 FBXW7
    nsv6751536copy number variation1nstd229human GRCh38 chr4: 152,367,940-152,384,971 , GRCh37.p13 chr4: 153,289,092-153,306,123 FBXW7
    nsv6751469copy number variation1nstd229human GRCh38 chr4: 152,448,673-152,486,620 , GRCh37.p13 chr4: 153,369,825-153,407,772 FBXW7
    nsv6751415copy number variation1nstd229human GRCh38 chr4: 152,391,697-152,391,791 , GRCh37.p13 chr4: 153,312,849-153,312,943 FBXW7
    nsv6751319copy number variation1nstd229human GRCh38 chr4: 152,441,580-152,564,339 , GRCh37.p13 chr4: 153,362,732-153,485,491 RPS3AP18, MIR4453HG, 3 more genes
    nsv6751101copy number variation1nstd229human GRCh38 chr4: 152,410,013-152,414,374 , GRCh37.p13 chr4: 153,331,165-153,335,526 FBXW7
    nsv6750744copy number variation1nstd229human GRCh38 chr4: 152,532,701-152,537,100 , GRCh37.p13 chr4: 153,453,853-153,458,252 MIR4453, FBXW7, 1 more genes
    nsv6747128copy number variation1nstd229human GRCh38 chr4: 152,443,813-152,447,135 , GRCh37.p13 chr4: 153,364,965-153,368,287 FBXW7
    nsv6747011copy number variation1nstd229human GRCh38 chr4: 152,427,649-152,427,826 , GRCh37.p13 chr4: 153,348,801-153,348,978 FBXW7
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