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Items: 1 to 20 of 146

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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
    nsv5362720translocation1nstd200human GRCh38 chr5: 176,630,060-176,630,060 , GRCh38 chr5: 176,629,909-176,629,909 , GRCh37.p13 chr5: 176,056,910-176,056,910 , GRCh37.p13 chr5: 176,057,061-176,057,061 SNCB, EIF4E1B, 1 more genes
    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
    nsv4451087copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 175,875,407-177,036,017 , GRCh38.p12 chr5: 176,448,406-177,609,016 DBN1, F12, 36 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
    nsv4347913copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 175,843,728-180,703,728 , GRCh38.p12 chr5: 176,416,727-181,276,727 CANX, CLTB, 177 more genes
    nsv3961014inversion1nstd168human GRCh38 chr5: 176,018,591-177,972,451 , GRCh37.p13 chr5: 175,445,594-177,399,452 , CLTB, 65 more genes
    nsv3956895inversion1nstd168human GRCh38 chr5: 175,907,339-177,953,331 , GRCh37.p13 chr5: 175,334,342-177,380,332 , CLTB, 68 more genes
    nsv3924491copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-177,436,413 , GRCh38 chr5: 176,143,674-178,009,412 , NCBI36 chr5: 175,503,283-177,369,019 CDHR2, LOC105377752, 59 more genes
    nsv3924410copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,132,340-177,586,960 , GRCh37 chr5: 175,559,343-177,013,961 , NCBI36 chr5: 175,491,949-176,946,567 PDLIM7, MIR1271, 44 more genes
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