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Items: 1 to 20 of 108

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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
    nsv7059252inversion1nstd229human GRCh38 chr10: 106,216,129-112,495,031 , GRCh37.p13 chr10: 107,975,887-114,254,790 LOC105378482, DUSP5, 64 more genes
    nsv6893994copy number variation1nstd229human GRCh38 chr10: 106,937,001-106,979,900 , GRCh37.p13 chr10: 108,696,759-108,739,658 SORCS1, RNA5SP325
    nsv6887308copy number variation1nstd229human GRCh38 chr10: 106,083,314-108,338,154 , GRCh37.p13 chr10: 107,843,072-110,097,912 SORCS1, LOC105378469, 13 more genes
    nsv6880788copy number variation1nstd229human GRCh38 chr10: 106,715,597-106,972,009 , GRCh37.p13 chr10: 108,475,355-108,731,767 SORCS1, RNA5SP325
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6879955copy number variation1nstd229human GRCh38 chr10: 106,969,250-106,972,387 , GRCh37.p13 chr10: 108,729,008-108,732,145 SORCS1, RNA5SP325
    nsv6879750copy number variation1nstd229human GRCh38 chr10: 106,932,569-106,993,665 , GRCh37.p13 chr10: 108,692,327-108,753,423 SORCS1, RNA5SP325
    nsv6594084inversion1nstd223human GRCh38 chr10: 104,554,685-109,812,699 , GRCh37.p13 chr10: 106,314,443-111,572,457 LOC105378477, LOC105378469, 35 more genes
    nsv6579866inversion1nstd223human GRCh38 chr10: 105,937,471-107,267,814 , GRCh37.p13 chr10: 107,697,229-109,027,572 SORCS1, RPL23AP59, 7 more genes
    nsv6444799copy number variation1nstd223human GRCh38 chr10: 106,686,283-107,084,736 , GRCh37.p13 chr10: 108,446,041-108,844,494 SORCS1, RNA5SP325
    nsv6436928copy number variation1nstd223human GRCh38 chr10: 106,969,250-106,972,387 , GRCh37.p13 chr10: 108,729,008-108,732,145 SORCS1, RNA5SP325
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6314068copy number variation1nstd102humanUncertain significance GRCh37 chr10: 108,039,346-109,787,835 , GRCh38.p12 chr10: 106,279,588-108,028,077 LOC105378473, RPL23AP59, 9 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6132014copy number variation1nstd213human GRCh37 chr10: 108,640,000-110,180,001 , GRCh38.p12 chr10: 106,880,242-108,420,243 SORCS1, RNA5SP325, 8 more genes
    nsv5968492inversion1nstd209human GRCh38 chr10: 104,554,685-109,812,698 , GRCh37.p13 chr10: 106,314,443-111,572,456 SORCS3, YWHAZP5, 35 more genes
    nsv4974023copy number variation1nstd200human GRCh38 chr10: 106,700,977-107,844,942 , GRCh37.p13 chr10: 108,460,735-109,604,700 RNA5SP325, LOC101927573, 4 more genes
    nsv4970512copy number variation1nstd200human GRCh38 chr10: 106,969,250-106,972,387 , GRCh37.p13 chr10: 108,729,008-108,732,145 RNA5SP325, SORCS1
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