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Items: 1 to 20 of 365

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097560copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 107,019,871-110,266,416 , GRCh38.p12 chr6: 106,571,996-109,945,213 ZPR1P1, OSTM1, 60 more genes
    nsv7055005inversion1nstd229human GRCh38 chr6: 108,167,886-110,172,775 , GRCh37.p13 chr6: 108,489,090-110,493,978 AK9, WASF1, 34 more genes
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6817143copy number variation1nstd229human GRCh38 chr6: 108,610,214-108,615,861 , GRCh37.p13 chr6: 108,931,417-108,937,064 FOXO3, SUMO2P8
    nsv6815225copy number variation1nstd229human GRCh38 chr6: 108,594,353-108,651,314 , GRCh37.p13 chr6: 108,915,556-108,972,517 FOXO3, SUMO2P8
    nsv6810306copy number variation1nstd229human GRCh38 chr6: 108,525,314-108,604,440 , GRCh37.p13 chr6: 108,846,517-108,925,643 AFG1L, FOXO3
    nsv6809452copy number variation1nstd229human GRCh38 chr6: 108,645,340-108,648,625 , GRCh37.p13 chr6: 108,966,543-108,969,828 FOXO3
    nsv6807485copy number variation1nstd229human GRCh38 chr6: 108,632,329-108,632,871 , GRCh37.p13 chr6: 108,953,532-108,954,074 FOXO3
    nsv6804977copy number variation1nstd229human GRCh38 chr6: 108,586,441-108,591,628 , GRCh37.p13 chr6: 108,907,644-108,912,831 FOXO3
    nsv6804847copy number variation1nstd229human GRCh38 chr6: 105,481,597-109,225,980 , GRCh37.p13 chr6: 105,929,472-109,547,183 LINC02836, SOBP, 61 more genes
    nsv6803164copy number variation1nstd229human GRCh38 chr6: 108,636,112-108,640,784 , GRCh37.p13 chr6: 108,957,315-108,961,987 FOXO3
    nsv6803061copy number variation1nstd229human GRCh38 chr6: 108,669,843-108,670,026 , GRCh37.p13 chr6: 108,991,046-108,991,229 FOXO3
    nsv6610400copy number variation1nstd223human GRCh38 chr6: 108,633,068-108,633,401 , GRCh37.p13 chr6: 108,954,271-108,954,604 FOXO3
    nsv6604845copy number variation1nstd223human GRCh38 chr6: 108,521,418-108,568,632 , GRCh37.p13 chr6: 108,842,621-108,889,835 FOXO3, AFG1L
    nsv6601283copy number variation1nstd223human GRCh38 chr6: 108,591,086-108,593,004 , GRCh37.p13 chr6: 108,912,289-108,914,207 FOXO3
    nsv6568800inversion1nstd223human GRCh38 chr6: 108,600,392-108,601,016 , GRCh37.p13 chr6: 108,921,595-108,922,219 FOXO3
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6294811mobile element insertion1nstd186human GRCh37 chr6: 108,923,760-108,923,811 , GRCh38.p12 chr6: 108,602,557-108,602,608 FOXO3
    nsv6140871copy number variation1nstd206human GRCh38 chr6: 108,683,694-108,683,956 , GRCh37.p13 chr6: 109,004,897-109,005,159 FOXO3
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