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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4716479copy number variation3nstd102humanPathogenic, Likely pathogenic GRCh37 chr16: 14,017,229-14,022,884 , GRCh38 chr16: 13,923,372-13,929,027 ERCC4
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4682745copy number variation1nstd102humanUncertain significance GRCh37 chr16: 13,915,808-14,031,725 , GRCh38.p12 chr16: 13,821,951-13,937,868 LOC105371093, ERCC4, 1 more genes
    nsv4632474copy number variation1nstd183human GRCh37 chr16: 13,812,690-14,070,525 , GRCh38.p12 chr16: 13,718,833-13,976,668 ERCC4, RPS26P52, 1 more genes
    nsv4627179copy number variation1nstd183human GRCh37 chr16: 14,042,967-14,049,734 , GRCh38.p12 chr16: 13,949,110-13,955,877 ERCC4
    nsv4455610copy number variation1nstd102humanUncertain significance GRCh37 chr16: 13,108,953-14,168,353 , GRCh38.p12 chr16: 13,015,096-14,074,496 LOC105371093, LINC02185, 8 more genes
    nsv4454746copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,014,013-14,042,214 , GRCh38 chr16: 13,920,156-13,948,357 RPS26P52, ERCC4
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4386008copy number variation1nstd173human GRCh37 chr16: 14,045,140-14,336,830 , GRCh38.p12 chr16: 13,951,283-14,242,973 MRTFB, TVP23CP2, 3 more genes
    nsv4244553copy number variation1nstd166human GRCh37.p13 chr16: 13,948,797-14,175,007 , GRCh38.p12 chr16: 13,854,940-14,081,150 ERCC4, MRTFB, 4 more genes
    nsv4235132copy number variation1nstd166human GRCh37.p13 chr16: 14,024,192-14,026,788 , GRCh38.p12 chr16: 13,930,335-13,932,931 ERCC4
    nsv3918893copy number variation1nstd102humanBenign NCBI36 chr16: 13,923,497-13,958,522 , GRCh37 chr16: 14,015,996-14,051,021 , GRCh38 chr16: 13,922,139-13,957,164 ERCC4, RPS26P52
    nsv3918732copy number variation1nstd102humanPathogenic GRCh37 chr16: 12,061,688-15,256,745 , GRCh38 chr16: 11,967,831-15,162,888 , NCBI36 chr16: 11,969,189-15,164,246 LOC105371087, BFAR, 62 more genes
    nsv3917207copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 11,953,825-15,187,557 , GRCh37 chr16: 12,046,324-15,280,056 , GRCh38 chr16: 11,952,467-15,186,199 TNFRSF17, ERCC4, 63 more genes
    nsv3915829copy number variation1nstd102humanPathogenic NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961 RPL35AP34, LOC100505915, 429 more genes
    nsv3910441copy number variation1nstd102humanPathogenic NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820 LOC729945, LOC102723728, 450 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS53, LINC02134, 1868 more genes
    nsv3906603copy number variation1nstd102humanUncertain significance GRCh37 chr16: 13,889,247-14,163,635 , GRCh38.p12 chr16: 13,795,390-14,069,778 MRTFB, ERCC4, 4 more genes
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