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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096810copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,456,384-49,459,947 , GRCh38.p12 chr3: 49,418,951-49,422,514 AMT, NICN1
    nsv7052450inversion1nstd229human GRCh38 chr3: 49,345,298-49,450,163 , GRCh37.p13 chr3: 49,382,731-49,487,596 TCTA, NICN1, 3 more genes
    nsv7040357inversion1nstd229human GRCh38 chr3: 49,317,804-49,472,849 , GRCh37.p13 chr3: 49,355,237-49,510,282 AMT, NICN1, 6 more genes
    nsv6707335copy number variation1nstd229human GRCh38 chr3: 49,312,201-49,508,500 , GRCh37.p13 chr3: 49,349,634-49,545,933 DAG1, NICN1, 6 more genes
    nsv6704811copy number variation1nstd229human GRCh38 chr3: 49,389,220-49,423,495 , GRCh37.p13 chr3: 49,426,653-49,460,928 NICN1, AMT, 2 more genes
    nsv6701570copy number variation1nstd229human GRCh38 chr3: 49,365,701-49,450,100 , GRCh37.p13 chr3: 49,403,134-49,487,533 NICN1, AMT, 2 more genes
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6367330copy number variation1nstd223human GRCh38 chr3: 49,398,077-49,478,018 , GRCh37.p13 chr3: 49,435,510-49,515,451 TCTA, RHOA, 4 more genes
    nsv6357395copy number variation1nstd223human GRCh38 chr3: 49,400,087-49,427,518 , GRCh37.p13 chr3: 49,437,520-49,464,951 AMT, TCTA, 2 more genes
    nsv6313476copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,060,512-49,678,685 , GRCh38.p12 chr3: 49,023,079-49,641,252 DAG1, GPX1, 23 more genes
    nsv6311988copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,454,201-49,457,785 , GRCh38.p12 chr3: 49,416,768-49,420,352 TCTA, NICN1, 1 more genes
    nsv6311878copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,394,821-49,459,947 , GRCh38.p12 chr3: 49,357,388-49,422,514 AMT, RHOA, 3 more genes
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5994118copy number variation1nstd212human GRCh38 chr3: 49,426,593-49,426,668 , GRCh37.p13 chr3: 49,464,026-49,464,101 NICN1
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5201436copy number variation1nstd204human GRCh37.p13 chr3: 49,439,734-49,516,233 , GRCh38.p13 chr3: 49,402,301-49,478,800 AMT, RHOA, 4 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
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