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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093699copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,747,968-103,535,657 , GRCh38.p12 chr10: 100,988,211-101,775,900 RNY5P7, TLX1, 25 more genes
    nsv7065586inversion1nstd229human GRCh38 chr10: 101,749,664-101,755,295 , GRCh37.p13 chr10: 103,509,421-103,515,052 LOC105378458
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897727copy number variation1nstd229human GRCh38 chr10: 101,666,701-101,878,800 , GRCh37.p13 chr10: 103,426,458-103,638,557 , LOC105378457, 10 more genes
    nsv6896227copy number variation1nstd229human GRCh38 chr10: 101,762,885-101,766,235 , GRCh37.p13 chr10: 103,522,642-103,525,992 LOC105378458, LOC105378457
    nsv6896140copy number variation1nstd229human GRCh38 chr10: 101,730,601-101,735,500 , GRCh37.p13 chr10: 103,490,358-103,495,257 LOC105378458
    nsv6893451copy number variation1nstd229human GRCh38 chr10: 101,742,587-101,746,061 , GRCh37.p13 chr10: 103,502,344-103,505,818 LOC105378458
    nsv6889353copy number variation1nstd229human GRCh38 chr10: 101,749,205-101,758,826 , GRCh37.p13 chr10: 103,508,962-103,518,583 LOC105378458
    nsv6888488copy number variation1nstd229human GRCh38 chr10: 101,752,101-101,754,600 , GRCh37.p13 chr10: 103,511,858-103,514,357 LOC105378458
    nsv6886921copy number variation1nstd229human GRCh38 chr10: 101,741,118-101,745,350 , GRCh37.p13 chr10: 103,500,875-103,505,107 LOC105378458
    nsv6886137copy number variation1nstd229human GRCh38 chr10: 101,764,816-101,789,165 , GRCh37.p13 chr10: 103,524,573-103,548,922 OGA, LOC105378457, 3 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6593133inversion1nstd223human GRCh38 chr10: 101,750,527-101,750,824 , GRCh37.p13 chr10: 103,510,284-103,510,581 LOC105378458
    nsv6591371inversion1nstd223human GRCh38 chr10: 101,755,714-101,756,982 , GRCh37.p13 chr10: 103,515,471-103,516,739 LOC105378458
    nsv6590678inversion1nstd223human GRCh38 chr10: 101,734,710-101,735,537 , GRCh37.p13 chr10: 103,494,467-103,495,294 LOC105378458
    nsv6580907inversion1nstd223human GRCh38 chr10: 101,737,724-101,738,167 , GRCh37.p13 chr10: 103,497,481-103,497,924 LOC105378458
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