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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5302598copy number variation1nstd204human GRCh38.p13 chr3: 109,643,426-112,176,826 , GRCh37.p13 chr3: 109,362,273-111,895,673 , NECTIN3-AS1, 28 more genes
    nsv5229675copy number variation1nstd204human GRCh38.p13 chr3: 111,834,401-112,176,600 , GRCh37.p13 chr3: 111,553,248-111,895,447 TMPRSS7, PLCXD2, 10 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919555copy number variation1nstd200human GRCh38 chr3: 112,121,028-112,127,518 , GRCh37.p13 chr3: 111,839,875-111,846,365 GCSAM, C3orf52
    nsv4914627copy number variation1nstd200human GRCh38 chr3: 109,643,716-112,176,659 , GRCh37.p13 chr3: 109,362,563-111,895,506 , NECTIN3, 28 more genes
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4806765copy number variation1nstd200human GRCh37 chr3: 111,839,875-111,846,365 , GRCh38.p12 chr3|NW_019805492.1: 4,318-10,808 , GRCh38.p12 chr3: 112,121,028-112,127,518 GCSAM, C3orf52
    nsv4794283copy number variation1nstd200human GRCh37 chr3: 109,362,563-111,895,506 , GRCh38.p12 chr3: 109,643,716-112,176,659 , LOC107984087, 28 more genes
    nsv4674254copy number variation1nstd102humanPathogenic GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638 IFT57, LINC00636, 111 more genes
    nsv4587014copy number variation1nstd183human GRCh37 chr3: 111,851,817-111,923,659 , GRCh38.p12 chr3: 112,132,970-112,204,812 , GRCh38.p12 chr3|NW_019805492.1: 16,260-97,550 INAVAP1, TBILA, 3 more genes
    nsv4468540mobile element insertion1nstd166human GRCh37.p13 chr3: 111,850,498-111,850,498 , GRCh38.p12 chr3: 112,131,651-112,131,651 , GRCh38.p12 chr3|NW_019805492.1: 14,941-14,941 C3orf52, GCSAM, 1 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv4074813copy number variation1nstd166human GRCh37.p13 chr3: 111,839,875-111,846,365 , GRCh38.p12 chr3|NW_019805492.1: 4,318-10,808 , GRCh38.p12 chr3: 112,121,028-112,127,518 C3orf52, GCSAM
    nsv3965819insertion1nstd168human GRCh37.p13 chr3: 111,782,184-111,918,788 , GRCh38 chr3: 112,063,337-112,199,941 C3orf52, GCSAM, 5 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
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 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
    nsv3913319copy number variation1nstd102humanPathogenic NCBI36 chr3: 105,822,754-117,295,421 , GRCh38 chr3: 104,621,220-116,093,884 , GRCh37 chr3: 104,340,064-115,812,731 TAGLN3, LINC00635, 151 more genes
    nsv3913048copy number variation1nstd102humanPathogenic NCBI36 chr3: 109,444,109-117,370,868 , GRCh38 chr3: 108,242,572-116,169,331 , GRCh37 chr3: 107,961,419-115,888,178 RPSAP29, DIMT1P1, 115 more genes
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