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Items: 1 to 20 of 422

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057629inversion1nstd229human GRCh38 chr5: 181,006,988-181,070,179 , GRCh37.p13 chr5: 180,433,988-180,497,179 BTNL3, BTNL9, 3 more genes
    nsv7055207inversion1nstd229human GRCh38 chr5: 180,875,426-181,038,549 , GRCh37.p13 chr5: 180,302,426-180,465,549 TMEM69P2, ARPP19P1, 6 more genes
    nsv7054793inversion1nstd229human GRCh38 chr5: 180,916,922-181,085,872 , GRCh37.p13 chr5: 180,343,922-180,512,872 RPS29P12, RPL13P10, 8 more genes
    nsv7053892inversion1nstd229human GRCh38 chr5: 181,052,018-181,072,264 , GRCh37.p13 chr5: 180,479,018-180,499,264 RPL13P10, BTNL9
    nsv7053423inversion1nstd229human GRCh38 chr5: 180,767,059-181,141,901 , GRCh37.p13 chr5: 180,194,059-180,568,901 HEIH, TRV-CAC1-3, 19 more genes
    nsv7045576inversion1nstd229human GRCh38 chr5: 180,805,627-181,281,045 , GRCh37.p13 chr5: 180,232,627-180,708,046 RPL13P10, TRV-AAC1-3, 46 more genes
    nsv7044540inversion1nstd229human GRCh38 chr5: 180,832,761-181,281,244 , GRCh37.p13 chr5: 180,259,761-180,708,245 LOC100128762, SNORD95, 44 more genes
    nsv7044050inversion1nstd229human GRCh38 chr5: 181,033,738-181,211,611 , GRCh37.p13 chr5: 180,460,738-180,638,611 TRP-TGG3-1, BTNL9, 24 more genes
    nsv7043722inversion1nstd229human GRCh38 chr5: 181,060,568-181,100,669 , GRCh37.p13 chr5: 180,487,568-180,527,669 TRL-AAG1-1, TRV-CAC1-3, 5 more genes
    nsv6797230copy number variation1nstd229human GRCh38 chr5: 180,905,901-181,039,300 , GRCh37.p13 chr5: 180,332,901-180,466,300 BTNL3, BTNL9, 6 more genes
    nsv6796121copy number variation1nstd229human GRCh38 chr5: 181,053,351-181,054,065 , GRCh37.p13 chr5: 180,480,351-180,481,065 BTNL9
    nsv6793524copy number variation1nstd229human GRCh38 chr5: 181,061,314-181,065,629 , GRCh37.p13 chr5: 180,488,314-180,492,629 BTNL9, RPL13P10
    nsv6792551copy number variation1nstd229human GRCh38 chr5: 181,053,385-181,208,980 , GRCh37.p13 chr5: 180,480,385-180,635,980 TRL-AAG1-2, OR2V1, 23 more genes
    nsv6787737copy number variation1nstd229human GRCh38 chr5: 181,052,896-181,052,935 , GRCh37.p13 chr5: 180,479,896-180,479,935 BTNL9
    nsv6785858copy number variation1nstd229human GRCh38 chr5: 181,037,739-181,037,888 , GRCh37.p13 chr5: 180,464,739-180,464,888 BTNL9
    nsv6784981copy number variation1nstd229human GRCh38 chr5: 180,850,968-181,155,283 , GRCh37.p13 chr5: 180,277,968-180,582,283 RNU6-1036P, LOC729707, 17 more genes
    nsv6781743copy number variation1nstd229human GRCh38 chr5: 181,013,625-181,062,196 , GRCh37.p13 chr5: 180,440,625-180,489,196 MIR8089, BTNL9
    nsv6781484copy number variation1nstd229human GRCh38 chr5: 181,026,140-181,057,268 , GRCh37.p13 chr5: 180,453,140-180,484,268 BTNL9, MIR8089
    nsv6778472copy number variation1nstd229human GRCh38 chr5: 181,018,155-181,074,841 , GRCh37.p13 chr5: 180,445,155-180,501,841 MIR8089, BTNL9, 1 more genes
    nsv6636938copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,922,498-180,608,605 , GRCh38.p12 chr5: 180,495,498-181,181,605 RNU6-1036P, TRL-AAG7-1, 34 more genes
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