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Items: 1 to 20 of 99

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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
    nsv6888502copy number variation1nstd229human GRCh38 chr10: 102,831,087-102,831,123 , GRCh37.p13 chr10: 104,590,844-104,590,880 CYP17A1-AS1, CYP17A1
    nsv6883614copy number variation1nstd229human GRCh38 chr10: 102,834,153-102,848,574 , GRCh37.p13 chr10: 104,593,910-104,608,331 PFN1P11, CYP17A1, 2 more genes
    nsv6586045inversion1nstd223human GRCh38 chr10: 102,827,986-102,829,163 , GRCh37.p13 chr10: 104,587,743-104,588,920 CYP17A1
    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
    nsv6308898copy number variation1nstd102humanPathogenic GRCh37 chr10: 104,592,258-104,597,718 , GRCh38.p12 chr10: 102,832,501-102,837,961 CYP17A1-AS1, CYP17A1
    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
    nsv6088314insertion1nstd212human GRCh38 chr10: 102,829,950-102,829,950 , GRCh37.p13 chr10: 104,589,707-104,589,707 CYP17A1
    nsv5507325copy number variation1nstd206human GRCh38 chr10: 102,828,010-102,828,753 , GRCh37.p13 chr10: 104,587,767-104,588,510 CYP17A1
    nsv4829703copy number variation1nstd200human GRCh37 chr10: 104,588,780-104,589,587 , GRCh38.p12 chr10: 102,829,023-102,829,830 CYP17A1
    nsv4679283copy number variation1nstd189human GRCh37.p13 chr10: 104,468,424-105,156,097 , GRCh38.p12 chr10: 102,708,667-103,396,340 , ARL3, 25 more genes
    nsv4389533copy number variation1nstd171human GRCh37 chr10: 104,590,837-104,590,871 , GRCh38.p12 chr10: 102,831,080-102,831,114 CYP17A1, CYP17A1-AS1
    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
    nsv4191024copy number variation1nstd166human GRCh37.p13 chr10: 104,593,910-104,608,284 , GRCh38.p12 chr10: 102,834,153-102,848,527 , CYP17A1-AS1, 3 more genes
    nsv3941947copy number variation1nstd167human GRCh37 chr10: 104,590,836-104,590,871 , GRCh38.p12 chr10: 102,831,079-102,831,114 CYP17A1, CYP17A1-AS1
    nsv3924696copy number variation1nstd102humanPathogenic GRCh38 chr10: 102,243,341-103,929,730 , GRCh37 chr10: 104,003,098-105,689,488 , NCBI36 chr10: 103,993,088-105,679,478 MIR146B, RPL23AP58, 48 more genes
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