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Items: 1 to 20 of 390

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv6837963copy number variation1nstd229human GRCh38 chr7: 77,541,268-77,542,426 , GRCh37.p13 chr7: 77,170,585-77,171,743 PTPN12
    nsv6835499copy number variation1nstd229human GRCh38 chr7: 77,345,101-77,620,000 , GRCh37.p13 chr7: 76,974,418-77,249,317 GCNT1P5, PTPN12, 2 more genes
    nsv6833482copy number variation1nstd229human GRCh38 chr7: 77,586,443-77,586,471 , GRCh37.p13 chr7: 77,215,760-77,215,788 PTPN12
    nsv6832980copy number variation1nstd229human GRCh38 chr7: 77,575,725-77,579,012 , GRCh37.p13 chr7: 77,205,042-77,208,329 PTPN12
    nsv6828694copy number variation1nstd229human GRCh38 chr7: 77,581,273-77,581,462 , GRCh37.p13 chr7: 77,210,590-77,210,779 PTPN12
    nsv6828604copy number variation1nstd229human GRCh38 chr7: 77,567,405-77,745,003 , GRCh37.p13 chr7: 77,196,722-77,374,320 LOC105375363, RSBN1L, 2 more genes
    nsv6826228copy number variation1nstd229human GRCh38 chr7: 77,472,122-77,600,620 , GRCh37.p13 chr7: 77,101,439-77,229,937 PTPN12
    nsv6825143copy number variation1nstd229human GRCh38 chr7: 77,613,695-77,716,233 , GRCh37.p13 chr7: 77,243,012-77,345,550 PTPN12, RSBN1L, 2 more genes
    nsv6824718copy number variation1nstd229human GRCh38 chr7: 77,561,384-77,561,572 , GRCh37.p13 chr7: 77,190,701-77,190,889 PTPN12
    nsv6821343copy number variation1nstd229human GRCh38 chr7: 77,564,979-77,565,072 , GRCh37.p13 chr7: 77,194,296-77,194,389 PTPN12
    nsv6818709copy number variation1nstd229human GRCh38 chr7: 74,993,422-78,510,839 , GRCh37.p13 chr7: 75,921,853-78,140,156 TMEM120A, LOC105375359, 75 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
    nsv6619657copy number variation1nstd223human GRCh38 chr7: 77,541,268-77,542,425 , GRCh37.p13 chr7: 77,170,585-77,171,742 PTPN12
    nsv6615708copy number variation1nstd223human GRCh38 chr7: 77,345,101-77,620,000 , GRCh37.p13 chr7: 76,974,418-77,249,317 GCNT1P5, LOC101927243, 2 more genes
    nsv6614795copy number variation1nstd223human GRCh38 chr7: 77,565,928-77,566,356 , GRCh37.p13 chr7: 77,195,245-77,195,673 PTPN12
    nsv6614074copy number variation1nstd223human GRCh38 chr7: 77,552,932-77,553,312 , GRCh37.p13 chr7: 77,182,249-77,182,629 PTPN12
    nsv6613225copy number variation1nstd223human GRCh38 chr7: 77,604,354-77,605,565 , GRCh37.p13 chr7: 77,233,671-77,234,882 PTPN12
    nsv6606893copy number variation1nstd223human GRCh38 chr7: 77,520,975-77,581,052 , GRCh37.p13 chr7: 77,150,292-77,210,369 PTPN12
    nsv6574095inversion1nstd223human GRCh38 chr7: 77,582,114-77,582,688 , GRCh37.p13 chr7: 77,211,431-77,212,005 PTPN12
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