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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959274insertion1nstd209human GRCh38 chr1: 167,889,442-167,889,442 , GRCh37.p13 chr1: 167,858,680-167,858,680 ADCY10
    nsv5886479copy number variation1nstd209human GRCh38 chr1: 167,913,652-167,913,729 , GRCh37.p13 chr1: 167,882,890-167,882,967 ADCY10
    nsv5874043copy number variation1nstd209human GRCh38 chr1: 167,897,696-167,898,015 , GRCh37.p13 chr1: 167,866,934-167,867,253 ADCY10
    nsv5720831mobile element insertion1nstd211human GRCh38 chr1: 167,819,147-167,819,147 , GRCh37.p13 chr1: 167,788,385-167,788,385 ADCY10
    nsv5717830mobile element insertion1nstd211human GRCh38 chr1: 167,842,639-167,842,639 , GRCh37.p13 chr1: 167,811,877-167,811,877 ADCY10
    nsv5677471mobile element insertion2nstd211human GRCh38 chr1: 167,889,451-167,889,451 , GRCh37.p13 chr1: 167,858,689-167,858,689 ADCY10
    nsv5615779insertion1nstd207human GRCh38 chr1: 167,889,442-167,889,442 , GRCh37.p13 chr1: 167,858,680-167,858,680 ADCY10
    nsv5580594copy number variation1nstd207human GRCh38 chr1: 167,897,705-167,898,023 , GRCh37.p13 chr1: 167,866,943-167,867,261 ADCY10
    nsv5554669mobile element insertion1nstd206human GRCh38 chr1: 167,819,147-167,819,197 , GRCh37.p13 chr1: 167,788,385-167,788,435 ADCY10
    nsv5431370copy number variation1nstd206human GRCh38 chr1: 167,897,288-167,898,018 , GRCh37.p13 chr1: 167,866,526-167,867,256 ADCY10
    nsv5417773copy number variation1nstd206human GRCh38 chr1: 167,913,656-167,913,730 , GRCh37.p13 chr1: 167,882,894-167,882,968 ADCY10
    nsv5399291mobile element insertion1nstd206human GRCh38 chr1: 167,889,442-167,889,442 , GRCh37.p13 chr1: 167,858,680-167,858,680 ADCY10
    nsv5385390mobile element deletion1nstd186human GRCh37 chr1: 167,866,951-167,867,256 , GRCh38.p12 chr1: 167,897,713-167,898,018 ADCY10
    nsv5382612mobile element deletion1nstd186human GRCh37 chr1: 167,866,951-167,867,255 , GRCh38.p12 chr1: 167,897,713-167,898,017 ADCY10
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5379119translocation1nstd200human GRCh38 chr1: 167,897,664-167,897,664 , GRCh38 chr21: 27,554,677-27,554,677 , GRCh37.p13 chr1: 167,866,902-167,866,902 , GRCh37.p13 chr21: 28,926,996-28,926,996 ADCY10
    nsv5353995translocation1nstd200human GRCh38 chr1: 167,913,730-167,913,730 , GRCh38 chr1: 167,913,656-167,913,656 , GRCh37.p13 chr1: 167,882,968-167,882,968 , GRCh37.p13 chr1: 167,882,894-167,882,894 ADCY10
    nsv5353994translocation1nstd200human GRCh38 chr1: 167,883,062-167,883,062 , GRCh38 chr1: 167,882,976-167,882,976 , GRCh37.p13 chr1: 167,852,214-167,852,214 , GRCh37.p13 chr1: 167,852,300-167,852,300 ADCY10
    nsv5342325translocation1nstd200human GRCh37 chr1: 167,882,968-167,882,968 , GRCh37 chr1: 167,882,894-167,882,894 , GRCh38.p12 chr1: 167,913,730-167,913,730 , GRCh38.p12 chr1: 167,913,656-167,913,656 ADCY10
    nsv5327725translocation1nstd204human GRCh38.p13 chr1: 167,913,730-167,913,730 , GRCh38.p13 chr1: 167,913,656-167,913,656 , GRCh37.p13 chr1: 167,882,894-167,882,894 , GRCh37.p13 chr1: 167,882,968-167,882,968 ADCY10
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