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Items: 1 to 20 of 122

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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
    nsv7093856copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,262,628-104,309,873 , GRCh38.p12 chr10: 102,502,871-102,550,116 SUFU, ACTR1A
    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
    nsv6895309copy number variation1nstd229human GRCh38 chr10: 102,480,383-102,524,772 , GRCh37.p13 chr10: 104,240,140-104,284,529 MFSD13A, SUFU, 1 more genes
    nsv6881005copy number variation1nstd229human GRCh38 chr10: 102,448,401-102,495,500 , GRCh37.p13 chr10: 104,208,158-104,255,257 ACTR1A, MFSD13A, 2 more genes
    nsv6879948copy number variation1nstd229human GRCh38 chr10: 102,485,735-102,488,149 , GRCh37.p13 chr10: 104,245,492-104,247,906 ACTR1A
    nsv6637556copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,031,306-104,366,150 , GRCh38.p12 chr10: 102,271,549-102,606,393 CUEDC2, C10orf95, 12 more genes
    nsv6584958inversion1nstd223human GRCh38 chr10: 102,478,056-102,478,641 , GRCh37.p13 chr10: 104,237,813-104,238,398 MFSD13A, ACTR1A
    nsv6580453inversion1nstd223human GRCh38 chr10: 102,495,651-102,496,005 , GRCh37.p13 chr10: 104,255,408-104,255,762 ACTR1A
    nsv6448470copy number variation1nstd223human GRCh38 chr10: 102,441,225-102,487,982 , GRCh37.p13 chr10: 104,200,982-104,247,739 ACTR1A, C10orf95, 2 more genes
    nsv6308975copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr10: 104,262,628-104,595,248 , GRCh38.p12 chr10: 102,502,871-102,835,491 ARL3, SUFU, 10 more genes
    nsv6131926copy number variation1nstd213human GRCh37 chr10: 103,560,000-105,280,001 , GRCh38.p12 chr10: 101,800,243-103,520,244 ARL3, CYP17A1, 56 more genes
    nsv6131924copy number variation1nstd213human GRCh37 chr10: 104,257,516-104,494,897 , GRCh38.p12 chr10: 102,497,759-102,735,140 ARL3, ACTR1A, 6 more genes
    nsv5963075insertion1nstd209human GRCh38 chr10: 102,493,001-102,493,001 , GRCh37.p13 chr10: 104,252,758-104,252,758 ACTR1A
    nsv4973992copy number variation1nstd200human GRCh38 chr10: 102,441,225-102,487,983 , GRCh37.p13 chr10: 104,200,982-104,247,740 ACTR1A, C10orf95, 2 more genes
    nsv4774820mobile element deletion1nstd200human GRCh37 chr10: 104,238,353-104,238,650 , GRCh38.p12 chr10: 102,478,596-102,478,893 ACTR1A, MFSD13A
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
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