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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7047168inversion1nstd229human GRCh38 chr3: 98,270,010-99,398,075 , GRCh37.p13 chr3: 97,988,854-99,116,919 OR5K2, RPL38P4, 24 more genes
    nsv7046246inversion1nstd229human GRCh38 chr3: 98,222,641-99,359,746 , GRCh37.p13 chr3: 97,941,485-99,078,590 LOC105374004, UBFD1P1, 28 more genes
    nsv7041727inversion1nstd229human GRCh38 chr3: 94,070,424-99,088,195 , GRCh37.p13 chr3: 93,789,268-98,807,039 LINC00973, OR5H7P, 63 more genes
    nsv6718071copy number variation1nstd229human GRCh38 chr3: 98,138,513-98,369,776 , GRCh37.p13 chr3: 97,857,357-98,088,620 LOC105374000, OR5K4, 14 more genes
    nsv6713827copy number variation1nstd229human GRCh38 chr3: 98,237,015-98,479,435 , GRCh37.p13 chr3: 97,955,859-98,198,279 LOC105373999, OR5H2, 9 more genes
    nsv6712762copy number variation1nstd229human GRCh38 chr3: 96,620,998-98,689,220 , GRCh37.p13 chr3: 96,339,842-98,408,064 GPR15, OR5K1, 41 more genes
    nsv6636842copy number variation1nstd102humanUncertain significance GRCh37 chr3: 97,283,117-98,218,677 , GRCh38.p12 chr3: 97,564,273-98,499,833 LOC105373997, LOC105374000, 31 more genes
    nsv6629073copy number variation1nstd224human GRCh37 chr3: 97,279,087-98,073,637 , GRCh38.p12 chr3: 97,560,243-98,354,793 OR5H1, OR5H5P, 26 more genes
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6375576copy number variation1nstd223human GRCh38 chr3: 98,138,513-98,369,776 , GRCh37.p13 chr3: 97,857,357-98,088,620 OR5H7P, LOC105373997, 14 more genes
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv5173893mobile element insertion1nstd203human GRCh38 chr3: 98,353,519-98,353,532 , GRCh37.p13 chr3: 98,072,363-98,072,376 OR5K4
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4919060copy number variation1nstd200human GRCh38 chr3: 97,824,265-98,358,535 , GRCh37.p13 chr3: 97,543,109-98,077,379 OR5AC2, OR5H8, 23 more genes
    nsv4887622inversion1nstd200human GRCh37 chr3: 94,357,590-100,127,961 , GRCh38.p12 chr3: 94,638,746-100,409,117 , CPOX, 82 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797634copy number variation1nstd200human GRCh37 chr3: 98,070,051-98,075,395 , GRCh38.p12 chr3: 98,351,207-98,356,551 OR5K4
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