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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899764copy number variation1nstd209human GRCh37.p13 chr5: 180,634,147-180,653,657 , GRCh38 chr5: 181,207,147-181,226,657 TRV-AAC1-4, TRIM7, 6 more genes
    nsv5893603copy number variation1nstd209human GRCh38 chr5: 181,208,256-181,208,309 , GRCh37.p13 chr5: 180,635,256-180,635,309 TRK-CTT2-2, TRIM7
    nsv5841970copy number variation1nstd209human GRCh38 chr5: 181,207,201-181,212,962 , GRCh37.p13 chr5: 180,634,201-180,639,962 TRIM7, TRA-TGC3-1, 1 more genes
    nsv5570059copy number variation1nstd207human GRCh38 chr5: 181,208,256-181,208,309 , GRCh37.p13 chr5: 180,635,256-180,635,309 TRIM7, TRK-CTT2-2
    nsv5239224copy number variation1nstd204human GRCh38.p13 chr5: 181,143,301-181,215,400 , GRCh37.p13 chr5: 180,570,301-180,642,400 TRK-CTT2-2, LINC01962, 14 more genes
    nsv4949326copy number variation1nstd200human GRCh38 chr5: 181,206,218-181,227,034 , GRCh37.p13 chr5: 180,633,218-180,654,034 TRIM7, MIR4638, 6 more genes
    nsv4828433copy number variation1nstd200human GRCh37 chr5: 180,633,218-180,654,034 , GRCh38.p12 chr5: 181,206,218-181,227,034 MIR4638, TRIM41, 6 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
    nsv4741210copy number variation1nstd199human GRCh37 chr5: 180,635,269-180,635,324 , GRCh38.p12 chr5: 181,208,269-181,208,324 TRK-CTT2-2, TRIM7
    nsv4729100copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,533,007-180,719,789 , GRCh38.p12 chr5: 181,106,007-181,292,788 TRV-AAC1-4, TRIM7-AS2, 27 more genes
    nsv4728969copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,064,955-180,719,789 , GRCh38.p12 chr5: 180,637,955-181,292,788 TMEM69P2, OR2V1, 52 more genes
    nsv4675041copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,479,838-180,695,063 , GRCh38.p12 chr5: 180,052,838-181,268,062 OR2AI1P, SNORD96A, 64 more genes
    nsv4655436copy number variation1nstd186human GRCh37 chr5: 180,635,257-180,635,310 , GRCh38.p12 chr5: 181,208,257-181,208,310 TRIM7, TRK-CTT2-2
    nsv4455497copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,848,982-180,719,789 , GRCh38.p12 chr5: 177,421,981-181,292,788 HEIH, MGAT4B, 149 more genes
    nsv4406656copy number variation1nstd174human GRCh37 chr5: 180,522,765-180,656,128 , GRCh38.p12 chr5: 181,095,765-181,229,128 TRV-AAC1-3, OR2V1, 26 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
    nsv4350315copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 177,776,148-180,687,012 , GRCh38.p12 chr5: 178,349,147-181,260,011 CANX, FOXO1B, 114 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
    nsv4114621copy number variation1nstd166human GRCh37.p13 chr5: 180,631,103-180,633,074 , GRCh38.p12 chr5: 181,204,103-181,206,074 TRIM7, TRA-TGC3-1, 1 more genes
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
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