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Items: 1 to 20 of 187

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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
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6896473copy number variation1nstd229human GRCh38 chr10: 100,042,916-100,046,922 , GRCh37.p13 chr10: 101,802,673-101,806,679 CPN1
    nsv6882563copy number variation1nstd229human GRCh38 chr10: 100,052,419-100,057,602 , GRCh37.p13 chr10: 101,812,176-101,817,359 MTATP8P4, CPN1
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6588003inversion1nstd223human GRCh38 chr10: 100,042,113-100,042,816 , GRCh37.p13 chr10: 101,801,870-101,802,573 CPN1
    nsv6583828inversion1nstd223human GRCh38 chr10: 100,054,967-100,055,686 , GRCh37.p13 chr10: 101,814,724-101,815,443 MTATP8P4, CPN1
    nsv6581962inversion1nstd223human GRCh38 chr10: 100,068,049-100,068,459 , GRCh37.p13 chr10: 101,827,806-101,828,216 CPN1
    nsv6450531copy number variation1nstd223human GRCh38 chr10: 100,052,419-100,057,598 , GRCh37.p13 chr10: 101,812,176-101,817,355 CPN1, MTATP8P4
    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
    nsv5848494copy number variation1nstd209human GRCh38 chr10: 100,079,031-100,090,551 , GRCh37.p13 chr10: 101,838,788-101,850,308 CPN1
    nsv5717072mobile element insertion2nstd211human GRCh38 chr10: 100,078,220-100,078,220 , GRCh37.p13 chr10: 101,837,977-101,837,977 CPN1
    nsv5487407copy number variation1nstd206human GRCh38 chr10: 100,044,336-100,046,112 , GRCh37.p13 chr10: 101,804,093-101,805,869 CPN1
    nsv5370899translocation1nstd200human GRCh38 chr10: 100,068,214-100,068,214 , GRCh38 chr7: 102,137,816-102,137,816 , GRCh37.p13 chr10: 101,827,971-101,827,971 , GRCh37.p13 chr7|NW_003571037.1: 62,146-62,146 , GRCh37.p13 chr7: 101,781,096-101,781,096 CUX1, CPN1
    nsv5343529translocation1nstd200human GRCh37 chr10: 101,827,971-101,827,971 , GRCh37 chr7: 101,781,096-101,781,096 , GRCh38.p12 chr10: 100,068,214-100,068,214 , GRCh38.p12 chr7: 102,137,816-102,137,816 CUX1, CPN1
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