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Items: 1 to 20 of 162

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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
    nsv5842523copy number variation1nstd209human GRCh38 chr5: 181,222,027-181,225,926 , GRCh37.p13 chr5: 180,649,027-180,652,926 TRIM41, TRV-CAC1-5, 2 more genes
    nsv5196441mobile element insertion1nstd203human GRCh38 chr5: 181,225,328-181,225,328 , GRCh37.p13 chr5: 180,652,328-180,652,328 TRIM41
    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
    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
    nsv4597983copy number variation1nstd183human GRCh37 chr5: 180,663,035-180,790,320 , GRCh38.p12 chr5: 181,236,035-181,363,319 , TRIM41, 12 more genes
    nsv4597982copy number variation1nstd183human GRCh37 chr5: 180,661,259-180,712,285 , GRCh38.p12 chr5: 181,234,259-181,285,284 RACK1, TRIM52, 5 more genes
    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
    nsv4394460copy number variation1nstd174human GRCh37 chr5: 180,663,035-180,719,790 , GRCh38.p12 chr5: 181,236,035-181,292,789 RACK1, TRIM52, 5 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
    nsv4339361sequence alteration1nstd166human GRCh37.p13 chr5: 180,649,490-180,731,391 , GRCh38.p12 chr5: 181,222,490-181,304,390 , TRIM52, 10 more genes
    nsv4123982copy number variation1nstd166human GRCh37.p13 chr5: 180,650,161-180,672,068 , GRCh38.p12 chr5: 181,223,161-181,245,068 SNORD96A, TRIM41, 3 more genes
    nsv3965058copy number variation1nstd168human GRCh38 chr5: 181,232,725-181,456,273 , GRCh37.p13 chr5: 180,659,725-180,883,274 , TRIM52, 13 more genes
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