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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074587inversion1nstd229human GRCh38 chr13: 88,216,554-90,380,882 , GRCh37.p13 chr13: 88,868,809-91,033,136 MIR622, LINC01047, 21 more genes
    nsv7067043inversion1nstd229human GRCh38 chr13: 88,254,077-90,389,586 , GRCh37.p13 chr13: 88,906,332-91,041,840 KRT18P27, LINC00559, 19 more genes
    nsv7063899inversion1nstd229human GRCh38 chr13: 87,663,888-92,195,406 , GRCh37.p13 chr13: 88,316,143-92,847,659 RNU6-75P, LOC105370311, 50 more genes
    nsv7062771inversion1nstd229human GRCh38 chr13: 86,949,883-89,810,099 , GRCh37.p13 chr13: 87,602,138-90,462,353 LINC00433, LOC105370302, 25 more genes
    nsv7062399inversion1nstd229human GRCh38 chr13: 87,893,483-90,331,274 , GRCh37.p13 chr13: 88,545,738-90,983,528 RPL29P29, KRT18P27, 22 more genes
    nsv6954310copy number variation1nstd229human GRCh38 chr13: 88,605,653-88,627,230 , GRCh37.p13 chr13: 89,257,908-89,279,484 LINC00560
    nsv6953671copy number variation1nstd229human GRCh38 chr13: 88,564,761-88,903,352 , GRCh37.p13 chr13: 89,217,016-89,555,606 LINC00560
    nsv6953126copy number variation1nstd229human GRCh38 chr13: 88,555,001-88,668,800 , GRCh37.p13 chr13: 89,207,256-89,321,054 LINC00560
    nsv6951980copy number variation1nstd229human GRCh38 chr13: 88,549,270-88,724,730 , GRCh37.p13 chr13: 89,201,525-89,376,984 LINC00560
    nsv6948988copy number variation1nstd229human GRCh38 chr13: 88,630,860-88,630,903 , GRCh37.p13 chr13: 89,283,114-89,283,157 LINC00560
    nsv6945689copy number variation1nstd229human GRCh38 chr13: 88,390,664-89,711,413 , GRCh37.p13 chr13: 89,042,919-90,329,881 LINC01047, LINC00353, 11 more genes
    nsv6944522copy number variation1nstd229human GRCh38 chr13: 87,882,311-88,764,267 , GRCh37.p13 chr13: 88,534,566-89,416,521 TET1P1, RPL29P29, 3 more genes
    nsv6944164copy number variation1nstd229human GRCh38 chr13: 88,566,773-88,716,465 , GRCh37.p13 chr13: 89,219,028-89,368,719 LINC00560
    nsv6943717copy number variation1nstd229human GRCh38 chr13: 88,555,018-88,668,830 , GRCh37.p13 chr13: 89,207,273-89,321,084 LINC00560
    nsv6938536copy number variation1nstd229human GRCh38 chr13: 88,275,385-88,764,884 , GRCh37.p13 chr13: 88,927,640-89,417,138 LINC00433, LINC00560
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637507copy number variation1nstd102humanUncertain significance GRCh37 chr13: 86,667,980-91,833,689 , GRCh38.p12 chr13: 86,093,845-91,181,435 LINC00559, LOC105370304, 47 more genes
    nsv6637451copy number variation1nstd102humanUncertain significance GRCh37 chr13: 85,665,879-90,460,716 , GRCh38.p12 chr13: 85,091,744-89,808,462 LINC00373, LINC00375, 37 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622334copy number variation2nstd224human GRCh37 chr13: 89,222,603-89,302,824 , GRCh38.p12 chr13: 88,570,348-88,650,570 LINC00560
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