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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv4949249copy number variation1nstd200human GRCh38 chr5: 176,347,453-176,410,835 , GRCh37.p13 chr5: 175,774,456-175,837,836 NOP16, KIAA1191, 4 more genes
    nsv4939973copy number variation1nstd200human GRCh38 chr5: 176,382,501-176,383,154 , GRCh37.p13 chr5: 175,809,504-175,810,157 ARL10, NOP16
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4765127inversion1nstd199human GRCh37 chr5: 175,457,760-177,239,501 , GRCh38.p12 chr5: 176,030,757-177,812,500 , CLTB, 60 more genes
    nsv4764354inversion1nstd199human GRCh37 chr5: 175,368,726-177,329,050 , GRCh38.p12 chr5: 175,941,723-177,902,049 , CLTB, 66 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4763338inversion1nstd199human GRCh37 chr5: 175,460,977-177,237,065 , GRCh38.p12 chr5: 176,033,974-177,810,064 , CLTB, 60 more genes
    nsv4755941inversion1nstd199human GRCh37 chr5: 175,346,194-177,347,044 , GRCh38.p12 chr5: 175,919,191-177,920,043 , CLTB, 66 more genes
    nsv4729600copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-177,114,151 , GRCh38.p12 chr5: 176,143,674-177,687,150 RNF44, NOP16, 48 more genes
    nsv4729439copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,394,616-177,436,413 , GRCh38.p12 chr5: 175,967,613-178,009,412 KIAA1191, DOK3, 65 more genes
    nsv4685982copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,346,695-177,469,711 , GRCh38.p12 chr5: 175,919,692-178,042,710 NOP16, DDX41, 65 more genes
    nsv4597916copy number variation1nstd183human GRCh37 chr5: 175,815,336-175,816,273 , GRCh38.p12 chr5: 176,388,335-176,389,272 NOP16, HIGD2A, 1 more genes
    nsv4590627copy number variation1nstd183human GRCh37 chr5: 175,469,507-175,886,627 , GRCh38.p12 chr5: 176,042,504-176,459,626 HIGD2A, MIR1271, 12 more genes
    nsv4455136copy number variation1nstd102humanUncertain significance GRCh37 chr5: 175,601,473-175,814,860 , GRCh38.p12 chr5: 176,174,470-176,387,859 KIAA1191, SIMC1, 7 more genes
    nsv4350559copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,990,352-180,690,937 , GRCh38.p12 chr5: 175,563,349-181,263,936 FAF2, ARL10, 198 more genes
    nsv4117755copy number variation1nstd166human GRCh37.p13 chr5: 175,810,770-175,810,879 , GRCh38.p12 chr5: 176,383,767-176,383,876 ARL10, NOP16
    nsv3961014inversion1nstd168human GRCh38 chr5: 176,018,591-177,972,451 , GRCh37.p13 chr5: 175,445,594-177,399,452 , CLTB, 65 more genes
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