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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115270mobile element insertion1nstd186human GRCh37 chr13: 103,435,913-103,435,913 , GRCh38.p12 chr13: 102,783,563-102,783,563 POGLUT2
    nsv5975558insertion1nstd209human GRCh38 chr13: 102,783,563-102,783,563 , GRCh37.p13 chr13: 103,435,913-103,435,913 POGLUT2
    nsv5713536mobile element insertion1nstd211human GRCh38 chr13: 102,796,312-102,796,312 , GRCh37.p13 chr13: 103,448,662-103,448,662 POGLUT2
    nsv5694868mobile element insertion2nstd211human GRCh38 chr13: 102,783,579-102,783,579 , GRCh37.p13 chr13: 103,435,929-103,435,929 POGLUT2
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5657537insertion1nstd207human GRCh38 chr13: 102,783,563-102,783,563 , GRCh37.p13 chr13: 103,435,913-103,435,913 POGLUT2
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5419563mobile element insertion1nstd206human GRCh38 chr13: 102,783,563-102,783,563 , GRCh37.p13 chr13: 103,435,913-103,435,913 POGLUT2
    nsv5313848copy number variation1nstd204human GRCh37.p13 chr13: 103,450,005-103,452,938 , GRCh38.p13 chr13: 102,797,655-102,800,588 POGLUT2, BIVM
    nsv5270317copy number variation1nstd204human GRCh38.p13 chr13: 102,798,208-102,800,689 , GRCh37.p13 chr13: 103,450,558-103,453,039 BIVM, POGLUT2
    nsv5140806mobile element insertion1nstd203human GRCh38 chr13: 102,783,563-102,783,579 , GRCh37.p13 chr13: 103,435,913-103,435,929 POGLUT2
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4993929copy number variation1nstd200human GRCh38 chr13: 102,777,238-103,138,970 , GRCh37.p13 chr13: 103,429,588-103,791,320 POGLUT2, RNY5P8, 5 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4847927copy number variation1nstd200human GRCh37 chr13: 103,439,675-103,440,966 , GRCh38.p12 chr13: 102,787,325-102,788,616 POGLUT2
    nsv4766820insertion1nstd199human GRCh37 chr13: 103,435,922-103,435,922 , GRCh38.p12 chr13: 102,783,572-102,783,572 POGLUT2
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 more genes
    nsv4724757insertion1nstd186human GRCh37 chr13: 103,435,913-103,435,913 , GRCh38.p12 chr13: 102,783,563-102,783,563 POGLUT2
    nsv4675892copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,240,346-106,103,782 , GRCh38.p12 chr13: 95,588,092-105,451,433 LOC105370328, LINC00554, 132 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
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