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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv6835945copy number variation1nstd229human GRCh38 chr7: 99,610,775-99,611,711 , GRCh37.p13 chr7: 99,208,398-99,209,334 TMEM225B
    nsv6833303copy number variation1nstd229human GRCh38 chr7: 99,563,414-99,570,547 , GRCh37.p13 chr7: 99,161,037-99,168,170 TMEM225B, ZNF655
    nsv6832679copy number variation1nstd229human GRCh38 chr7: 99,598,381-99,603,682 , GRCh37.p13 chr7: 99,196,004-99,201,305 TMEM225B
    nsv6831355copy number variation1nstd229human GRCh38 chr7: 99,601,808-99,632,035 , GRCh37.p13 chr7: 99,199,431-99,229,658 ZSCAN25, TMEM225B
    nsv6829860copy number variation1nstd229human GRCh38 chr7: 99,595,856-99,601,091 , GRCh37.p13 chr7: 99,193,479-99,198,714 TMEM225B
    nsv6826910copy number variation1nstd229human GRCh38 chr7: 99,583,012-99,725,447 , GRCh37.p13 chr7: 99,180,635-99,323,070 CYP3A51P, ZSCAN25, 5 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
    nsv6616759copy number variation1nstd223human GRCh38 chr7: 99,582,871-99,583,555 , GRCh37.p13 chr7: 99,180,494-99,181,178 TMEM225B
    nsv6611581copy number variation1nstd223human GRCh38 chr7: 99,589,701-99,598,900 , GRCh37.p13 chr7: 99,187,324-99,196,523 TMEM225B
    nsv6609152copy number variation1nstd223human GRCh38 chr7: 99,592,068-99,592,607 , GRCh37.p13 chr7: 99,189,691-99,190,230 TMEM225B
    nsv6607544copy number variation1nstd223human GRCh38 chr7: 99,587,483-99,587,988 , GRCh37.p13 chr7: 99,185,106-99,185,611 TMEM225B
    nsv6607492copy number variation1nstd223human GRCh38 chr7: 99,582,591-99,584,383 , GRCh37.p13 chr7: 99,180,214-99,182,006 TMEM225B
    nsv6607316copy number variation1nstd223human GRCh38 chr7: 99,593,201-99,598,000 , GRCh37.p13 chr7: 99,190,824-99,195,623 TMEM225B
    nsv6604659copy number variation1nstd223human GRCh38 chr7: 99,591,437-99,592,223 , GRCh37.p13 chr7: 99,189,060-99,189,846 TMEM225B
    nsv6604448copy number variation1nstd223human GRCh38 chr7: 99,590,789-99,591,612 , GRCh37.p13 chr7: 99,188,412-99,189,235 TMEM225B
    nsv6604062copy number variation1nstd223human GRCh38 chr7: 99,603,627-99,608,136 , GRCh37.p13 chr7: 99,201,250-99,205,759 TMEM225B
    nsv6573946inversion1nstd223human GRCh38 chr7: 99,576,929-99,577,338 , GRCh37.p13 chr7: 99,174,552-99,174,961 TMEM225B, ZNF655
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