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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971247insertion1nstd209human GRCh38 chr19: 35,067,064-35,067,064 , GRCh37.p13 chr19: 35,557,968-35,557,968 HPN, HPN-AS1
    nsv5941469copy number variation1nstd209human GRCh38 chr19: 35,045,650-35,045,718 , GRCh37.p13 chr19: 35,536,554-35,536,622 HPN
    nsv5930027copy number variation1nstd209human GRCh38 chr19: 35,040,155-35,040,237 , GRCh37.p13 chr19: 35,531,059-35,531,141 HPN, SCN1B
    nsv5649467insertion1nstd207human GRCh38 chr19: 35,067,064-35,067,064 , GRCh37.p13 chr19: 35,557,968-35,557,968 HPN, HPN-AS1
    nsv5597521copy number variation1nstd207human GRCh38 chr19: 35,045,650-35,045,718 , GRCh37.p13 chr19: 35,536,554-35,536,622 HPN
    nsv5525477copy number variation1nstd206human GRCh38 chr19: 35,040,157-35,040,230 , GRCh37.p13 chr19: 35,531,061-35,531,134 SCN1B, HPN
    nsv5520409copy number variation1nstd206human GRCh38 chr19: 35,056,258-35,056,696 , GRCh37.p13 chr19: 35,547,162-35,547,600 HPN
    nsv5197225mobile element insertion1nstd203human GRCh38 chr19: 35,046,803-35,046,811 , GRCh37.p13 chr19: 35,537,707-35,537,715 HPN
    nsv5027686copy number variation1nstd200human GRCh38 chr19: 35,064,339-35,065,053 , GRCh37.p13 chr19: 35,555,243-35,555,957 HPN-AS1, HPN
    nsv5027685copy number variation1nstd200human GRCh38 chr19: 35,052,292-35,053,473 , GRCh37.p13 chr19: 35,543,196-35,544,377 HPN
    nsv4749490copy number variation1nstd199human GRCh37 chr19: 35,536,583-35,536,651 , GRCh38.p12 chr19: 35,045,679-35,045,747 HPN
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4541487insertion1nstd166human GRCh37.p13 chr19: 35,557,968-35,557,968 , GRCh38.p12 chr19: 35,067,064-35,067,064 HPN-AS1, HPN
    nsv4457758copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,548,527-35,772,471 , GRCh38.p12 chr19: 35,057,623-35,281,568 LOC105372379, LSR, 15 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4271111copy number variation1nstd166human GRCh37.p13 chr19: 35,555,243-35,555,957 , GRCh38.p12 chr19: 35,064,339-35,065,053 HPN-AS1, HPN
    nsv4262401copy number variation1nstd166human GRCh37.p13 chr19: 35,547,162-35,547,600 , GRCh38.p12 chr19: 35,056,258-35,056,696 HPN
    nsv4258013copy number variation1nstd166human GRCh37.p13 chr19: 35,531,061-35,531,134 , GRCh38.p12 chr19: 35,040,157-35,040,230 HPN, SCN1B
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