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Items: 1 to 20 of 133

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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
    nsv7069448inversion1nstd229human GRCh38 chr10: 102,458,268-102,461,812 , GRCh37.p13 chr10: 104,218,025-104,221,569 MFSD13A
    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
    nsv6891085copy number variation1nstd229human GRCh38 chr10: 102,457,001-102,459,900 , GRCh37.p13 chr10: 104,216,758-104,219,657 MFSD13A
    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
    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
    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
    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
    nsv5130661mobile element insertion1nstd203human GRCh38 chr10: 102,467,011-102,467,027 , GRCh37.p13 chr10: 104,226,768-104,226,784 MFSD13A
    nsv4973993copy number variation1nstd200human GRCh38 chr10: 102,453,904-102,467,833 , GRCh37.p13 chr10: 104,213,661-104,227,590 C10orf95-AS1, MFSD13A
    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
    nsv4492194mobile element insertion1nstd166human GRCh37.p13 chr10: 104,223,421-104,223,421 , GRCh38.p12 chr10: 102,463,664-102,463,664 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
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
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