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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7097252copy number variation1nstd102humanPathogenic GRCh37 chr4: 493,125-663,896 , GRCh38.p12 chr4: 499,336-670,107 PDE6B, PIGG, 4 more genes
    nsv7097251copy number variation1nstd102humanUncertain significance GRCh37 chr4: 493,125-1,843,544 , GRCh38.p12 chr4: 499,336-1,841,817 PDE6B, LOC105374339, 44 more genes
    nsv7096733copy number variation1nstd102humanPathogenic GRCh37 chr4: 520,808-1,020,391 , GRCh38.p12 chr4: 527,019-1,026,603 PDE6B-AS1, PIGG, 19 more genes
    nsv7046852inversion1nstd229human GRCh38 chr4: 654,880-662,724 , GRCh37.p13 chr4: 648,669-656,513 PDE6B, PDE6B-AS1
    nsv6736703copy number variation1nstd229human GRCh38 chr4: 392,960-701,480 , GRCh37.p13 chr4: 507,005-695,269 PDE6B, SLC49A3, 11 more genes
    nsv6733132copy number variation1nstd229human GRCh38 chr4: 575,901-736,700 , GRCh37.p13 chr4: 569,690-730,489 MYL5, PDE6B-AS1, 6 more genes
    nsv6731830copy number variation1nstd229human GRCh38 chr4: 584,855-697,995 , GRCh37.p13 chr4: 578,644-691,784 PDE6B, MYL5, 4 more genes
    nsv6727715copy number variation1nstd229human GRCh38 chr4: 610,435-691,769 , GRCh37.p13 chr4: 604,224-685,558 MYL5, PDE6B-AS1, 3 more genes
    nsv6726676copy number variation1nstd229human GRCh38 chr4: 598,320-670,748 , GRCh37.p13 chr4: 592,109-664,537 ATP5ME, PDE6B, 1 more genes
    nsv6723619copy number variation1nstd229human GRCh38 chr4: 594,540-684,982 , GRCh37.p13 chr4: 588,329-678,771 PDE6B-AS1, MYL5, 3 more genes
    nsv6722636copy number variation1nstd229human GRCh38 chr4: 634,927-678,700 , GRCh37.p13 chr4: 628,716-672,489 MYL5, PDE6B-AS1, 3 more genes
    nsv6721213copy number variation1nstd229human GRCh38 chr4: 651,772-691,440 , GRCh37.p13 chr4: 645,561-685,229 SLC49A3, ATP5ME, 3 more genes
    nsv6636859copy number variation1nstd102humanUncertain significance GRCh37 chr4: 600,446-729,427 , GRCh38.p12 chr4: 606,657-735,638 PCGF3, SLC49A3, 4 more genes
    nsv6636691copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-2,437,290 , GRCh38.p12 chr4: 68,454-2,435,563 SPON2, TACC3, 77 more genes
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636256copy number variation1nstd102humanPathogenic GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377 AFAP1-AS1, LOC389199, 294 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
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