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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7076844inversion1nstd229human GRCh38 chr19: 35,026,104-35,028,708 , GRCh37.p13 chr19: 35,517,008-35,519,612 GRAMD1A, SCN1B
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002856copy number variation1nstd229human GRCh38 chr19: 35,031,334-35,031,443 , GRCh37.p13 chr19: 35,522,238-35,522,347 SCN1B
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6209284copy number variation1nstd214human GRCh38 chr19: 35,040,155-35,040,237 , GRCh37.p13 chr19: 35,531,059-35,531,141 HPN, SCN1B
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5939548copy number variation1nstd209human GRCh38 chr19: 35,028,834-35,029,123 , GRCh37.p13 chr19: 35,519,738-35,520,027 SCN1B
    nsv5930027copy number variation1nstd209human GRCh38 chr19: 35,040,155-35,040,237 , GRCh37.p13 chr19: 35,531,059-35,531,141 HPN, SCN1B
    nsv5525477copy number variation1nstd206human GRCh38 chr19: 35,040,157-35,040,230 , GRCh37.p13 chr19: 35,531,061-35,531,134 SCN1B, HPN
    nsv5375416translocation1nstd200human GRCh38 chr19: 35,030,475-35,030,475 , GRCh38 chr19: 35,030,557-35,030,557 , GRCh37.p13 chr19: 35,521,379-35,521,379 , GRCh37.p13 chr19: 35,521,461-35,521,461 SCN1B
    nsv5172837mobile element insertion1nstd203human GRCh38 chr19: 35,031,502-35,031,518 , GRCh37.p13 chr19: 35,522,406-35,522,422 SCN1B
    nsv4501885mobile element insertion1nstd166human GRCh37.p13 chr19: 35,522,406-35,522,406 , GRCh38.p12 chr19: 35,031,502-35,031,502 SCN1B
    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
    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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