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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6836568copy number variation1nstd229human GRCh38 chr7: 55,307,501-55,452,200 , GRCh37.p13 chr7: 55,375,194-55,519,893 LANCL2, LOC100129276, 1 more genes
    nsv6835071copy number variation1nstd229human GRCh38 chr7: 55,424,323-55,424,520 , GRCh37.p13 chr7: 55,492,016-55,492,213 LANCL2
    nsv6830530copy number variation1nstd229human GRCh38 chr7: 55,272,801-55,840,400 , GRCh37.p13 chr7: 55,340,494-55,908,093 SUMO2P3, LOC102723656, 20 more genes
    nsv6829809copy number variation1nstd229human GRCh38 chr7: 55,361,252-55,363,898 , GRCh37.p13 chr7: 55,428,945-55,431,591 LANCL2
    nsv6828363copy number variation1nstd229human GRCh38 chr7: 55,395,969-55,396,159 , GRCh37.p13 chr7: 55,463,662-55,463,852 LANCL2
    nsv6827467copy number variation1nstd229human GRCh38 chr7: 55,363,201-55,369,200 , GRCh37.p13 chr7: 55,430,894-55,436,893 LANCL2
    nsv6825757copy number variation1nstd229human GRCh38 chr7: 55,396,248-55,396,280 , GRCh37.p13 chr7: 55,463,941-55,463,973 LANCL2
    nsv6822233copy number variation1nstd229human GRCh38 chr7: 55,368,625-55,368,705 , GRCh37.p13 chr7: 55,436,318-55,436,398 LANCL2
    nsv6820159copy number variation1nstd229human GRCh38 chr7: 55,372,317-55,379,910 , GRCh37.p13 chr7: 55,440,010-55,447,603 LANCL2
    nsv6819624copy number variation1nstd229human GRCh38 chr7: 55,401,901-55,475,400 , GRCh37.p13 chr7: 55,469,594-55,543,093 VOPP1, LANCL2
    nsv6819204copy number variation1nstd229human GRCh38 chr7: 55,368,721-55,370,900 , GRCh37.p13 chr7: 55,436,414-55,438,593 LANCL2
    nsv6636595copy number variation1nstd102humanUncertain significance GRCh37 chr7: 53,991,820-56,148,011 , GRCh38.p12 chr7: 53,924,127-56,080,318 PSPH, SNORA22B, 46 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
    nsv6612482copy number variation1nstd223human GRCh38 chr7: 55,361,252-55,363,898 , GRCh37.p13 chr7: 55,428,945-55,431,591 LANCL2
    nsv6604878copy number variation1nstd223human GRCh38 chr7: 55,317,654-55,578,429 , GRCh37.p13 chr7: 55,385,347-55,646,122 VOPP1, LOC100129276, 2 more genes
    nsv6568616inversion1nstd223human GRCh38 chr7: 55,433,910-55,434,332 , GRCh37.p13 chr7: 55,501,603-55,502,025 LANCL2, VOPP1
    nsv6566470inversion1nstd223human GRCh38 chr7: 55,415,039-55,415,141 , GRCh37.p13 chr7: 55,482,732-55,482,834 LANCL2
    nsv6566345inversion1nstd223human GRCh38 chr7: 55,419,822-55,434,020 , GRCh37.p13 chr7: 55,487,515-55,501,713 VOPP1, LANCL2
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6303900copy number variation1nstd186human GRCh37 chr7: 55,436,318-55,436,398 , GRCh38.p12 chr7: 55,368,625-55,368,705 LANCL2
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