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Items: 1 to 20 of 94

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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
    nsv6704633copy number variation1nstd229human GRCh38 chr3: 99,819,504-99,820,713 , GRCh37.p13 chr3: 99,538,348-99,539,557 HP09053, CMSS1
    nsv6636951copy number variation1nstd102humanUncertain significance GRCh37 chr3: 99,428,530-99,586,184 , GRCh38.p12 chr3: 99,709,686-99,867,340 HP09053, CMSS1, 2 more genes
    nsv6629326copy number variation1nstd224human GRCh37 chr3: 99,442,745-99,906,993 , GRCh38.p12 chr3: 99,723,901-100,188,149 COL8A1, FILIP1L, 7 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
    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
    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
    nsv4919151copy number variation1nstd200human GRCh38 chr3: 99,710,948-99,994,408 , GRCh37.p13 chr3: 99,429,792-99,713,252 , COL8A1, 5 more genes
    nsv4914553copy number variation1nstd200human GRCh38 chr3: 99,823,128-99,893,492 , GRCh37.p13 chr3: 99,541,972-99,612,336 HP09053, FILIP1L, 1 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
    nsv4797673copy number variation1nstd200human GRCh37 chr3: 99,429,792-99,713,252 , GRCh38.p12 chr3: 99,710,948-99,994,408 , COL8A1, 5 more genes
    nsv4728581copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 95,563,096-102,371,126 , GRCh38.p12 chr3: 95,844,252-102,652,282 COL8A1, CPOX, 107 more genes
    nsv4712308copy number variation1nstd195human GRCh37 chr3: 99,538,465-99,538,466 , GRCh38.p12 chr3: 99,819,621-99,819,622 CMSS1, HP09053
    nsv3959684copy number variation1nstd168human GRCh38 chr3: 99,804,908-99,841,007 , GRCh37.p13 chr3: 99,523,752-99,559,851 CMSS1, FILIP1L, 1 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
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