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Items: 1 to 20 of 76

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978020insertion1nstd209human GRCh38 chr12: 12,914,549-12,914,549 , GRCh37.p13 chr12: 13,067,483-13,067,483 GPRC5A, MIR614
    nsv5913621copy number variation1nstd209human GRCh38 chr12: 12,916,808-12,927,052 , GRCh37.p13 chr12: 13,069,742-13,079,986 GPRC5A, GPRC5D-AS1
    nsv5863908copy number variation1nstd209human GRCh38 chr12: 12,916,738-12,924,110 , GRCh37.p13 chr12: 13,069,672-13,077,044 GPRC5A
    nsv5547965insertion1nstd206human GRCh38 chr12: 12,914,593-12,914,596 , GRCh37.p13 chr12: 13,067,527-13,067,530 GPRC5A, MIR614
    nsv5495738copy number variation1nstd206human GRCh38 chr12: 12,916,808-12,927,055 , GRCh37.p13 chr12: 13,069,742-13,079,989 GPRC5D-AS1, GPRC5A
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5137651mobile element insertion1nstd203human GRCh38 chr12: 12,895,821-12,895,843 , GRCh37.p13 chr12: 13,048,755-13,048,777 GPRC5A
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4974363copy number variation1nstd200human GRCh38 chr12: 12,916,808-12,927,055 , GRCh37.p13 chr12: 13,069,742-13,079,989 GPRC5A, GPRC5D-AS1
    nsv4972307copy number variation1nstd200human GRCh38 chr12: 12,895,761-12,900,689 , GRCh37.p13 chr12: 13,048,695-13,053,623 GPRC5A
    nsv4972306copy number variation1nstd200human GRCh38 chr12: 12,891,636-12,895,776 , GRCh37.p13 chr12: 13,044,570-13,048,710 GPRC5A
    nsv4972305copy number variation1nstd200human GRCh38 chr12: 12,879,337-12,905,016 , GRCh37.p13 chr12: 13,032,271-13,057,950 GPRC5A
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4848118copy number variation1nstd200human GRCh37 chr12: 13,048,695-13,053,623 , GRCh38.p12 chr12: 12,895,761-12,900,689 GPRC5A
    nsv4846053copy number variation1nstd200human GRCh37 chr12: 13,069,742-13,079,989 , GRCh38.p12 chr12: 12,916,808-12,927,055 GPRC5A, GPRC5D-AS1
    nsv4829830copy number variation1nstd200human GRCh37 chr12: 13,032,243-13,057,932 , GRCh38.p12 chr12: 12,879,309-12,904,998 GPRC5A
    nsv4682144copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr12: 12,869,936-14,135,064 , GRCh38.p12 chr12: 12,717,002-13,982,130 GPR19, EMP1, 26 more genes
    nsv4675174copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,737,824-16,780,886 , GRCh38.p12 chr12: 11,584,890-16,627,952 LOC107001063, RN7SKP162, 89 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
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