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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
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 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
    nsv7002869copy number variation1nstd229human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 IFNL4P1, IFNL4, 19 more genes
    nsv6998425copy number variation1nstd229human GRCh38 chr19: 38,900,571-38,930,432 , GRCh37.p13 chr19: 39,391,211-39,421,072 NFKBIB, CCER2, 2 more genes
    nsv6531882copy number variation1nstd223human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 NFKBIB, IFNL3, 19 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
    nsv6144358copy number variation1nstd206human GRCh38 chr19: 38,852,874-38,930,874 , GRCh37.p13 chr19: 39,343,514-39,421,514 NFKBIB, MRPS12, 4 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5973074insertion1nstd209human GRCh38 chr19: 38,929,261-38,929,261 , GRCh37.p13 chr19: 39,419,901-39,419,901 SARS2, MRPS12
    nsv5547110insertion1nstd206human GRCh38 chr19: 38,929,277-38,929,309 , GRCh37.p13 chr19: 39,419,917-39,419,949 MRPS12, SARS2
    nsv5533841copy number variation1nstd206human GRCh38 chr19: 38,925,137-38,929,107 , GRCh37.p13 chr19: 39,415,777-39,419,747 MRPS12, SARS2
    nsv5165369mobile element insertion1nstd203human GRCh38 chr19: 38,929,261-38,929,277 , GRCh37.p13 chr19: 39,419,901-39,419,917 SARS2, MRPS12
    nsv4621273copy number variation1nstd183human GRCh37 chr19: 39,415,233-39,482,669 , GRCh38.p12 chr19|NW_014040929.1: 334,265-401,701 , GRCh38.p12 chr19: 38,924,593-38,992,029 SARS2, MRPS12, 1 more genes
    nsv4546380insertion1nstd166human GRCh37.p13 chr19: 39,419,901-39,419,901 , GRCh38.p12 chr19|NW_014040929.1: 338,933-338,933 , GRCh38.p12 chr19: 38,929,261-38,929,261 SARS2, MRPS12
    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
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3912394copy number variation1nstd102humanUncertain significance NCBI36 chr19: 44,054,509-44,534,649 , GRCh37.p13 chr19: 39,362,669-39,842,809 , GRCh38.p12 chr19: 38,872,029-39,352,169 SAMD4B, IFNL1, 20 more genes
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