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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138569copy number variation1nstd232human GRCh37.p13 chr6: 110,775,820-110,775,887 , GRCh38.p12 chr6: 110,454,617-110,454,684 SLC22A16
    nsv7050442inversion1nstd229human GRCh38 chr6: 110,436,394-110,436,616 , GRCh37.p13 chr6: 110,757,597-110,757,819 SLC22A16
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7045135inversion1nstd229human GRCh38 chr6: 110,420,440-110,426,643 , GRCh37.p13 chr6: 110,741,643-110,747,846 SLC22A16, LOC105377936
    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
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6815267copy number variation1nstd229human GRCh38 chr6: 110,447,642-110,468,282 , GRCh37.p13 chr6: 110,768,845-110,789,485 SLC22A16
    nsv6811603copy number variation1nstd229human GRCh38 chr6: 110,465,401-110,473,600 , GRCh37.p13 chr6: 110,786,604-110,794,803 LOC105377938, SLC22A16
    nsv6808361copy number variation1nstd229human GRCh38 chr6: 110,460,428-110,460,535 , GRCh37.p13 chr6: 110,781,631-110,781,738 SLC22A16
    nsv6805752copy number variation1nstd229human GRCh38 chr6: 110,433,801-110,437,900 , GRCh37.p13 chr6: 110,755,004-110,759,103 SLC22A16
    nsv6799940copy number variation1nstd229human GRCh38 chr6: 110,419,101-110,422,680 , GRCh37.p13 chr6: 110,740,304-110,743,883 SLC22A16, LOC105377936
    nsv6799136copy number variation1nstd229human GRCh38 chr6: 110,326,547-111,405,944 , GRCh37.p13 chr6: 110,647,750-111,727,147 RPS19P5, REV3L, 30 more genes
    nsv6614143copy number variation1nstd223human GRCh38 chr6: 110,431,957-110,432,909 , GRCh37.p13 chr6: 110,753,160-110,754,112 SLC22A16
    nsv6609507copy number variation1nstd223human GRCh38 chr6: 110,460,303-110,460,873 , GRCh37.p13 chr6: 110,781,506-110,782,076 SLC22A16
    nsv6602804copy number variation1nstd223human GRCh38 chr6: 110,424,457-110,425,784 , GRCh37.p13 chr6: 110,745,660-110,746,987 SLC22A16
    nsv6570600inversion1nstd223human GRCh38 chr6: 110,420,437-110,426,643 , GRCh37.p13 chr6: 110,741,640-110,747,846 SLC22A16, LOC105377936
    nsv6567864inversion1nstd223human GRCh38 chr6: 109,778,846-111,235,585 , GRCh37.p13 chr6: 110,100,049-111,556,788 RNU6-1115P, GSTM2P1, 33 more genes
    nsv6315400copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,713,707-111,100,242 , GRCh38.p12 chr6: 110,392,504-110,779,039 RPS19P5, SLC22A16, 12 more genes
    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
    nsv6313613copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,472,732-114,762,836 , GRCh38.p12 chr6: 110,151,529-114,441,672 LOC107986522, TUBE1, 87 more genes
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