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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099198copy number variation1nstd231human GRCh38.p12 chr1: 44,129,375-46,768,878 , GRCh37 chr1: 44,595,047-47,234,550 PLK3, FAAH, 93 more genes
    nsv7095531copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,257,753-46,663,493 , GRCh38.p12 chr1: 43,792,082-46,197,821 AKR1A1, OSTCP5, 87 more genes
    nsv7058009inversion1nstd229human GRCh38 chr1: 44,481,832-44,481,875 , GRCh37.p13 chr1: 44,947,504-44,947,547 RNF220
    nsv7055071inversion1nstd229human GRCh38 chr1: 43,970,005-47,371,780 , GRCh37.p13 chr1: 44,435,677-47,837,452 SNORD38A, PPIAP36, 121 more genes
    nsv7054826inversion1nstd229human GRCh38 chr1: 43,915,848-44,729,930 , GRCh37.p13 chr1: 44,381,520-45,195,602 RNU5F-1, KLF18, 31 more genes
    nsv7053695inversion1nstd229human GRCh38 chr1: 44,514,581-44,518,937 , GRCh37.p13 chr1: 44,980,253-44,984,609 RNF220
    nsv7049976inversion1nstd229human GRCh38 chr1: 44,573,737-44,580,333 , GRCh37.p13 chr1: 45,039,409-45,046,005 RNF220
    nsv7047953inversion1nstd229human GRCh38 chr1: 44,574,862-44,574,915 , GRCh37.p13 chr1: 45,040,534-45,040,587 RNF220
    nsv7046836inversion1nstd229human GRCh38 chr1: 44,568,355-44,568,492 , GRCh37.p13 chr1: 45,034,027-45,034,164 RNF220
    nsv7040450inversion1nstd229human GRCh38 chr1: 44,428,894-44,428,956 , GRCh37.p13 chr1: 44,894,566-44,894,628 RNF220
    nsv7038412inversion1nstd229human GRCh38 chr1: 44,639,789-44,647,970 , GRCh37.p13 chr1: 45,105,461-45,113,642 LOC107984950, RNF220
    nsv6650458copy number variation1nstd229human GRCh38 chr1: 44,555,588-44,556,583 , GRCh37.p13 chr1: 45,021,260-45,022,255 RNF220
    nsv6650457copy number variation1nstd229human GRCh38 chr1: 44,550,622-44,554,243 , GRCh37.p13 chr1: 45,016,294-45,019,915 RNF220
    nsv6650456copy number variation1nstd229human GRCh38 chr1: 44,549,360-44,552,983 , GRCh37.p13 chr1: 45,015,032-45,018,655 RNF220
    nsv6650390copy number variation1nstd229human GRCh38 chr1: 44,577,960-44,578,052 , GRCh37.p13 chr1: 45,043,632-45,043,724 RNF220
    nsv6650389copy number variation1nstd229human GRCh38 chr1: 44,558,186-44,558,375 , GRCh37.p13 chr1: 45,023,858-45,024,047 RNF220
    nsv6650387copy number variation1nstd229human GRCh38 chr1: 44,413,847-44,417,305 , GRCh37.p13 chr1: 44,879,519-44,882,977 RNF220
    nsv6650385copy number variation1nstd229human GRCh38 chr1: 44,409,127-44,409,273 , GRCh37.p13 chr1: 44,874,799-44,874,945 RNF220
    nsv6650382copy number variation1nstd229human GRCh38 chr1: 44,352,620-44,465,082 , GRCh37.p13 chr1: 44,818,292-44,930,754 RNF220, RNU6-369P, 1 more genes
    nsv6650250copy number variation1nstd229human GRCh38 chr1: 44,534,126-44,547,587 , GRCh37.p13 chr1: 44,999,798-45,013,259 MIR5584, RNF220
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