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Items: 1 to 20 of 129

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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
    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
    nsv6889091copy number variation1nstd229human GRCh38 chr10: 100,450,246-100,462,128 , GRCh37.p13 chr10: 102,210,003-102,221,885 WNT8B
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6441680copy number variation1nstd223human GRCh38 chr10: 99,317,365-100,480,706 , GRCh37.p13 chr10: 101,077,122-102,240,463 WNT8B, GOT1, 29 more genes
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv5856944copy number variation1nstd209human GRCh38 chr10: 100,476,416-100,477,644 , GRCh37.p13 chr10: 102,236,173-102,237,401 , WNT8B
    nsv5489745copy number variation1nstd206human GRCh38 chr10: 100,454,549-100,509,731 , GRCh37.p13 chr10: 102,214,306-102,269,488 , SEC31B, 1 more genes
    nsv5189425mobile element insertion1nstd203human GRCh38 chr10: 100,467,324-100,467,342 , GRCh37.p13 chr10: 102,227,081-102,227,099 , WNT8B
    nsv5135751mobile element insertion1nstd203human GRCh38 chr10: 100,477,767-100,477,793 , GRCh37.p13 chr10: 102,237,524-102,237,550 , WNT8B
    nsv5129191mobile element insertion1nstd203human GRCh38 chr10: 100,474,574-100,474,582 , GRCh37.p13 chr10: 102,234,331-102,234,339 , WNT8B
    nsv4970293copy number variation1nstd200human GRCh38 chr10: 100,450,246-100,462,128 , GRCh37.p13 chr10: 102,210,003-102,221,885 , WNT8B
    nsv4836364copy number variation1nstd200human GRCh37 chr10: 102,214,306-102,269,488 , GRCh38.p12 chr10: 100,454,549-100,509,731 , WNT8B, 1 more genes
    nsv4674975copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,932,457-102,392,841 , GRCh38.p12 chr10: 100,172,700-100,633,084 NDUFB8, SNORA12, 12 more genes
    nsv4427025copy number variation1nstd174human GRCh37 chr10: 102,213,492-102,269,947 , GRCh38.p12 chr10: 100,453,735-100,510,190 , SEC31B, 1 more genes
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