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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5694560mobile element insertion1nstd211human GRCh38 chr10: 102,127,035-102,127,035 , GRCh37.p13 chr10: 103,886,792-103,886,792 PPRC1
    nsv5485240copy number variation1nstd206human GRCh38 chr10: 102,129,166-102,129,223 , GRCh37.p13 chr10: 103,888,923-103,888,980 PPRC1
    nsv5475661copy number variation1nstd206human GRCh38 chr10: 102,128,796-102,129,153 , GRCh37.p13 chr10: 103,888,553-103,888,910 PPRC1
    nsv5373276translocation1nstd200human GRCh38 chr10: 112,293,160-112,293,160 , GRCh38 chr10: 102,132,554-102,132,554 , GRCh37.p13 chr10: 114,052,918-114,052,918 , GRCh37.p13 chr10: 103,892,311-103,892,311 PPRC1, TECTB
    nsv5365062translocation1nstd200human GRCh38 chr10: 102,123,211-102,123,211 , GRCh38 chr10: 102,124,762-102,124,762 , GRCh37.p13 chr10: 103,882,968-103,882,968 , GRCh37.p13 chr10: 103,884,519-103,884,519 PPRC1
    nsv5365061translocation1nstd200human GRCh38 chr10: 102,122,711-102,122,711 , GRCh38 chr10: 102,124,765-102,124,765 , GRCh37.p13 chr10: 103,882,468-103,882,468 , GRCh37.p13 chr10: 103,884,522-103,884,522 PPRC1
    nsv5348054translocation1nstd200human GRCh38 chr10: 102,148,651-102,148,651 , GRCh38 chr10: 112,292,710-112,292,710 , GRCh37.p13 chr10: 103,908,408-103,908,408 , GRCh37.p13 chr10: 114,052,468-114,052,468 TECTB, PPRC1
    nsv5337025translocation1nstd200human GRCh37 chr10: 103,882,468-103,882,468 , GRCh37 chr10: 103,884,522-103,884,522 , GRCh38.p12 chr10: 102,122,711-102,122,711 , GRCh38.p12 chr10: 102,124,765-102,124,765 PPRC1
    nsv5333291translocation1nstd200human GRCh37 chr10: 103,884,519-103,884,519 , GRCh37 chr10: 103,882,968-103,882,968 , GRCh38.p12 chr10: 102,123,211-102,123,211 , GRCh38.p12 chr10: 102,124,762-102,124,762 PPRC1
    nsv5304042copy number variation1nstd204human GRCh38.p13 chr10: 101,912,568-102,213,549 , GRCh37.p13 chr10: 103,672,325-103,973,306 LDB1, PPRC1, 3 more genes
    nsv5244983copy number variation1nstd204human GRCh38.p13 chr10: 101,912,601-102,213,600 , GRCh37.p13 chr10: 103,672,358-103,973,357 NOLC1, LDB1, 3 more genes
    nsv5137084mobile element insertion1nstd203human GRCh38 chr10: 102,128,391-102,128,433 , GRCh37.p13 chr10: 103,888,148-103,888,190 PPRC1
    nsv4973989copy number variation1nstd200human GRCh38 chr10: 102,148,863-102,152,999 , GRCh37.p13 chr10: 103,908,620-103,912,756 PPRC1, NOLC1
    nsv4970349copy number variation1nstd200human GRCh38 chr10: 102,127,686-102,127,804 , GRCh37.p13 chr10: 103,887,443-103,887,561 PPRC1
    nsv4970348copy number variation1nstd200human GRCh38 chr10: 102,123,639-102,124,899 , GRCh37.p13 chr10: 103,883,396-103,884,656 PPRC1
    nsv4848963copy number variation1nstd200human GRCh37 chr10: 103,883,665-103,889,522 , GRCh38.p12 chr10: 102,123,908-102,129,765 PPRC1
    nsv4837851copy number variation1nstd200human GRCh37 chr10: 103,888,557-103,888,955 , GRCh38.p12 chr10: 102,128,800-102,129,198 PPRC1
    nsv4728795copy number variation1nstd102humanUncertain significance GRCh37 chr10: 103,582,453-103,931,269 , GRCh38.p12 chr10: 101,822,696-102,171,512 HPS6, NOLC1, 6 more genes
    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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