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Items: 1 to 20 of 553

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    nsv7094349copy number variation1nstd102humanUncertain significance GRCh37 chr14: 88,391,407-89,343,754 , GRCh38.p12 chr14: 87,925,063-88,877,410 LOC105370612, SPATA7, 15 more genes
    nsv7069334inversion1nstd229human GRCh38 chr14: 84,501,002-89,358,377 , GRCh37.p13 chr14: 84,967,346-89,824,721 EML5, LOC105370612, 35 more genes
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv6975823copy number variation1nstd229human GRCh38 chr14: 88,632,458-88,637,077 , GRCh37.p13 chr14: 89,098,802-89,103,421 EML5
    nsv6972889copy number variation1nstd229human GRCh38 chr14: 88,630,975-88,631,145 , GRCh37.p13 chr14: 89,097,319-89,097,489 EML5
    nsv6971281copy number variation1nstd229human GRCh38 chr14: 88,761,201-88,769,100 , GRCh37.p13 chr14: 89,227,545-89,235,444 EML5
    nsv6967626copy number variation1nstd229human GRCh38 chr14: 88,624,201-88,645,100 , GRCh37.p13 chr14: 89,090,545-89,111,444 ZC3H14, EML5
    nsv6965870copy number variation1nstd229human GRCh38 chr14: 88,751,963-88,752,134 , GRCh37.p13 chr14: 89,218,307-89,218,478 EML5
    nsv6965512copy number variation1nstd229human GRCh38 chr14: 88,636,821-88,637,018 , GRCh37.p13 chr14: 89,103,165-89,103,362 EML5
    nsv6964829copy number variation1nstd229human GRCh38 chr14: 88,663,654-88,679,529 , GRCh37.p13 chr14: 89,129,998-89,145,873 EML5
    nsv6964517copy number variation1nstd229human GRCh38 chr14: 88,623,501-88,685,500 , GRCh37.p13 chr14: 89,089,845-89,151,844 EML5, ZC3H14
    nsv6960478copy number variation1nstd229human GRCh38 chr14: 88,702,145-89,001,510 , GRCh37.p13 chr14: 89,168,489-89,467,854 EML5, TTC8, 1 more genes
    nsv6960107copy number variation1nstd229human GRCh38 chr14: 88,742,701-88,867,100 , GRCh37.p13 chr14: 89,209,045-89,333,444 TTC8, EML5, 1 more genes
    nsv6959604copy number variation1nstd229human GRCh38 chr14: 88,482,877-88,760,860 , GRCh37.p13 chr14: 88,949,221-89,227,204 ZC3H14, EML5, 3 more genes
    nsv6959129copy number variation1nstd229human GRCh38 chr14: 88,721,974-88,757,382 , GRCh37.p13 chr14: 89,188,318-89,223,726 EML5
    nsv6637996copy number variation1nstd102humanUncertain significance GRCh37 chr14: 85,366,999-90,760,040 , GRCh38.p12 chr14: 84,900,655-90,293,696 LOC105370608, FOXN3-AS2, 49 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
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