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Items: 1 to 20 of 326

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7137106copy number variation1nstd102humanUncertain significance GRCh37 chr7: 154,633,174-155,446,847 , GRCh38.p12 chr7: 154,841,464-155,654,153 RBM33, RBM33-DT, 21 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv7064624inversion1nstd229human GRCh38 chr7: 155,517,623-155,520,906 , GRCh37.p13 chr7: 155,310,318-155,313,601 CNPY1
    nsv6835287copy number variation1nstd229human GRCh38 chr7: 155,556,414-155,567,398 , GRCh37.p13 chr7: 155,349,109-155,360,093 CNPY1
    nsv6834022copy number variation1nstd229human GRCh38 chr7: 154,808,210-155,712,129 , GRCh37.p13 chr7: 154,599,920-155,504,823 RBM33, LOC105375594, 21 more genes
    nsv6828772copy number variation1nstd229human GRCh38 chr7: 155,558,242-155,558,604 , GRCh37.p13 chr7: 155,350,937-155,351,299 CNPY1
    nsv6824525copy number variation1nstd229human GRCh38 chr7: 152,687,878-156,500,924 , GRCh37.p13 chr7: 152,384,963-156,293,618 RN7SKP280, LINC03010, 44 more genes
    nsv6821276copy number variation1nstd229human GRCh38 chr7: 155,531,820-155,566,277 , GRCh37.p13 chr7: 155,324,515-155,358,972 CNPY1
    nsv6820373copy number variation1nstd229human GRCh38 chr7: 155,515,106-155,517,445 , GRCh37.p13 chr7: 155,307,801-155,310,140 CNPY1
    nsv6819994copy number variation1nstd229human GRCh38 chr7: 155,555,474-155,555,659 , GRCh37.p13 chr7: 155,348,169-155,348,354 CNPY1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6574535inversion1nstd223human GRCh38 chr7: 155,552,976-155,553,460 , GRCh37.p13 chr7: 155,345,671-155,346,155 CNPY1
    nsv6426918copy number variation1nstd223human GRCh38 chr7: 155,515,103-155,517,444 , GRCh37.p13 chr7: 155,307,798-155,310,139 CNPY1
    nsv6425863copy number variation1nstd223human GRCh38 chr7: 155,512,101-155,513,800 , GRCh37.p13 chr7: 155,304,796-155,306,495 CNPY1
    nsv6423983copy number variation1nstd223human GRCh38 chr7: 155,506,201-155,511,000 , GRCh37.p13 chr7: 155,298,896-155,303,695 CNPY1
    nsv6315413copy number variation1nstd102humanPathogenic GRCh37 chr7: 154,831,466-156,356,088 , GRCh38.p12 chr7: 155,039,756-156,563,394 SHH, INSIG1, 27 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
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