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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051182inversion1nstd229human GRCh38 chr7: 55,824,163-55,828,049 , GRCh37.p13 chr7: 55,891,856-55,895,742 SEPTIN14
    nsv6838051copy number variation1nstd229human GRCh38 chr7: 55,822,497-55,822,573 , GRCh37.p13 chr7: 55,890,190-55,890,266 SEPTIN14
    nsv6834298copy number variation1nstd229human GRCh38 chr7: 55,769,234-56,068,384 , GRCh37.p13 chr7: 55,836,927-56,136,077 ZNF713, LOC101409255, 12 more genes
    nsv6834280copy number variation1nstd229human GRCh38 chr7: 55,788,501-55,797,800 , GRCh37.p13 chr7: 55,856,194-55,865,493 SEPTIN14, RNU6-1126P, 1 more genes
    nsv6833222copy number variation1nstd229human GRCh38 chr7: 55,839,725-55,857,022 , GRCh37.p13 chr7: 55,907,418-55,924,715 SEPTIN14
    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
    nsv6830510copy number variation1nstd229human GRCh38 chr7: 55,806,751-55,808,799 , GRCh37.p13 chr7: 55,874,444-55,876,492 LOC100420540, SEPTIN14
    nsv6830200copy number variation1nstd229human GRCh38 chr7: 55,789,506-55,798,819 , GRCh37.p13 chr7: 55,857,199-55,866,512 RNU6-1126P, CICP12, 1 more genes
    nsv6830114copy number variation1nstd229human GRCh38 chr7: 55,787,234-55,793,126 , GRCh37.p13 chr7: 55,854,927-55,860,819 RNU6-1126P, SEPTIN14
    nsv6828695copy number variation1nstd229human GRCh38 chr7: 55,793,897-55,804,490 , GRCh37.p13 chr7: 55,861,590-55,872,183 CICP12, SEPTIN14
    nsv6826712copy number variation1nstd229human GRCh38 chr7: 55,796,302-55,806,076 , GRCh37.p13 chr7: 55,863,995-55,873,769 CICP12, SEPTIN14
    nsv6824841copy number variation1nstd229human GRCh38 chr7: 55,789,515-55,793,577 , GRCh37.p13 chr7: 55,857,208-55,861,270 RNU6-1126P, SEPTIN14
    nsv6823794copy number variation1nstd229human GRCh38 chr7: 55,713,901-56,129,100 , GRCh37.p13 chr7: 55,781,594-56,196,793 SEPTIN14, LOC100419984, 23 more genes
    nsv6821085copy number variation1nstd229human GRCh38 chr7: 55,814,301-55,897,700 , GRCh37.p13 chr7: 55,881,994-55,965,393 SEPTIN14, ZNF713, 1 more genes
    nsv6819736copy number variation1nstd229human GRCh38 chr7: 55,860,034-55,868,840 , GRCh37.p13 chr7: 55,927,727-55,936,533 SEPTIN14
    nsv6819180copy number variation1nstd229human GRCh38 chr7: 55,838,901-55,859,200 , GRCh37.p13 chr7: 55,906,594-55,926,893 SEPTIN14
    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
    nsv6619460copy number variation1nstd223human GRCh38 chr7: 55,839,721-55,857,017 , GRCh37.p13 chr7: 55,907,414-55,924,710 SEPTIN14
    nsv6619435copy number variation1nstd223human GRCh38 chr7: 55,806,901-55,808,400 , GRCh37.p13 chr7: 55,874,594-55,876,093 SEPTIN14
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