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Items: 1 to 20 of 135

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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
    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
    nsv6717206copy number variation1nstd229human GRCh38 chr3: 98,121,124-98,260,725 , GRCh37.p13 chr3: 97,839,968-97,979,569 OR5H1, OR5H15, 9 more genes
    nsv6713931copy number variation1nstd229human GRCh38 chr3: 98,143,680-98,218,449 , GRCh37.p13 chr3: 97,862,524-97,937,293 OR5H5P, OR5H15, 5 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
    nsv6701142copy number variation1nstd229human GRCh38 chr3: 98,114,001-98,174,700 , GRCh37.p13 chr3: 97,832,845-97,893,544 POU5F1P7, OR5H1, 3 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
    nsv6629075copy number variation1nstd224human GRCh37 chr3: 97,851,841-97,867,846 , GRCh38.p12 chr3: 98,132,997-98,149,002 OR5H14, LOC105373996, 1 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
    nsv5837480copy number variation1nstd209human GRCh38 chr3: 98,132,683-98,154,365 , GRCh37.p13 chr3: 97,851,527-97,873,209 OR5H1, OR5H14, 1 more genes
    nsv5442602copy number variation1nstd206human GRCh38 chr3: 98,132,800-98,169,574 , GRCh37.p13 chr3: 97,851,644-97,888,418 OR5H1, LOC105373996, 2 more genes
    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
    nsv4919074copy number variation1nstd200human GRCh38 chr3: 98,133,461-98,169,382 , GRCh37.p13 chr3: 97,852,305-97,888,226 OR5H14, OR5H15, 2 more genes
    nsv4919073copy number variation1nstd200human GRCh38 chr3: 98,127,451-98,162,857 , GRCh37.p13 chr3: 97,846,295-97,881,701 OR5H1, LOC105373996, 1 more genes
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