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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5944943copy number variation1nstd209human GRCh38 chr13: 31,132,567-31,133,397 , GRCh37.p13 chr13: 31,706,704-31,707,534 HSPH1
    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
    nsv5505959copy number variation1nstd206human GRCh38 chr13: 31,135,289-31,135,388 , GRCh37.p13 chr13: 31,709,426-31,709,525 HSPH1
    nsv5501707copy number variation1nstd206human GRCh38 chr13: 31,151,681-31,314,087 , GRCh37.p13 chr13: 31,725,818-31,888,224 HSPH1, LOC105370148, 2 more genes
    nsv5155500mobile element insertion1nstd203human GRCh38 chr13: 31,146,193-31,146,209 , GRCh37.p13 chr13: 31,720,330-31,720,346 HSPH1
    nsv5144156mobile element insertion1nstd203human GRCh38 chr13: 31,143,998-31,144,013 , GRCh37.p13 chr13: 31,718,135-31,718,150 HSPH1
    nsv5004455copy number variation1nstd200human GRCh38 chr13: 31,151,681-31,314,087 , GRCh37.p13 chr13: 31,725,818-31,888,224 B3GLCT, ANKRD26P4, 2 more genes
    nsv4829700copy number variation1nstd200human GRCh37 chr13: 31,725,817-31,888,225 , GRCh38.p12 chr13: 31,151,680-31,314,088 B3GLCT, ANKRD26P4, 2 more genes
    nsv4611821copy number variation1nstd183human GRCh37 chr13: 31,726,099-31,885,812 , GRCh38.p12 chr13: 31,151,962-31,311,675 B3GLCT, ANKRD26P4, 2 more genes
    nsv4574500mobile element insertion1nstd166human GRCh37.p13 chr13: 31,707,573-31,707,573 , GRCh38.p12 chr13: 31,133,436-31,133,436 HSPH1
    nsv4513785mobile element insertion1nstd166human GRCh37.p13 chr13: 31,718,135-31,718,135 , GRCh38.p12 chr13: 31,143,998-31,143,998 HSPH1
    nsv4429128copy number variation1nstd174human GRCh37 chr13: 31,725,532-31,893,030 , GRCh38.p12 chr13: 31,151,395-31,318,893 HSPH1, B3GLCT, 2 more genes
    nsv4379184copy number variation1nstd173human GRCh37 chr13: 31,726,086-31,885,812 , GRCh38.p12 chr13: 31,151,949-31,311,675 B3GLCT, LOC105370148, 2 more genes
    nsv4371942copy number variation1nstd173human GRCh37 chr13: 31,726,086-31,890,969 , GRCh38.p12 chr13: 31,151,949-31,316,832 HSPH1, LOC105370148, 2 more genes
    nsv4366952copy number variation1nstd173human GRCh37 chr13: 31,725,374-31,890,969 , GRCh38.p12 chr13: 31,151,237-31,316,832 ANKRD26P4, B3GLCT, 2 more genes
    nsv4230465copy number variation1nstd166human GRCh37.p13 chr13: 31,718,478-31,718,566 , GRCh38.p12 chr13: 31,144,341-31,144,429 HSPH1
    nsv4218262copy number variation1nstd166human GRCh37.p13 chr13: 31,725,785-31,888,224 , GRCh38.p12 chr13: 31,151,648-31,314,087 B3GLCT, ANKRD26P4, 2 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924246copy number variation1nstd102humanPathogenic NCBI36 chr13: 29,785,946-38,739,818 , GRCh37 chr13: 30,887,946-39,841,818 , GRCh38 chr13: 30,313,809-39,267,681 LINC01048, N4BP2L2-IT2, 117 more genes
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