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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381799copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 11,348,700-11,349,387 , GRCh38.p12 chr16: 11,254,843-11,255,530 SOCS1, LOC105371082
    nsv4992715copy number variation1nstd200human GRCh38 chr16: 11,254,995-11,255,228 , GRCh37.p13 chr16: 11,348,852-11,349,085 LOC105371082, SOCS1
    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
    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
    nsv4680676copy number variation1nstd189human GRCh37.p13 chr16: 11,333,398-11,784,674 , GRCh38.p12 chr16: 11,239,541-11,690,818 , PRM1, 15 more genes
    nsv4679254copy number variation1nstd189human GRCh37.p13 chr16: 11,247,365-11,544,021 , GRCh38.p12 chr16: 11,153,508-11,450,165 PRM1, PRM2, 12 more genes
    nsv4678852copy number variation1nstd189human GRCh37.p13 chr16: 11,303,331-11,581,403 , GRCh38.p12 chr16: 11,209,474-11,487,547 PRM1, PRM2, 12 more genes
    nsv4627808copy number variation1nstd183human GRCh37 chr16: 11,348,209-11,349,009 , GRCh38.p12 chr16: 11,254,352-11,255,152 LOC105371082, SOCS1
    nsv4626696copy number variation1nstd183human GRCh37 chr16: 11,349,044-11,350,944 , GRCh38.p12 chr16: 11,255,187-11,257,087 SOCS1, LOC105371082
    nsv4623099copy number variation1nstd183human GRCh37 chr16: 11,348,965-11,352,749 , GRCh38.p12 chr16: 11,255,108-11,258,892 SOCS1, LOC105371082
    nsv4455459copy number variation1nstd102humanUncertain significance GRCh37 chr16: 11,124,777-11,387,164 , GRCh38.p12 chr16: 11,030,920-11,293,307 LOC105371081, CLEC16A, 8 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4249713copy number variation1nstd166human GRCh37.p13 chr16: 11,334,665-11,437,694 , GRCh38.p12 chr16: 11,240,808-11,343,837 PRM3, TNP2, 8 more genes
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 METRN, FAM234A, 413 more genes
    nsv3917929copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873 LOC100130283, PGP, 386 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
    nsv3913858copy number variation1nstd102humanPathogenic GRCh37 chr16: 73,141-11,390,552 , GRCh38 chr16: 23,141-11,296,695 , NCBI36 chr16: 13,141-11,298,053 TPSP1, LUC7L, 382 more genes
    nsv3910449copy number variation1nstd102humanUncertain significance NCBI36 chr16: 11,194,565-11,362,521 , GRCh37.p13 chr16: 11,287,064-11,455,020 , GRCh38.p12 chr16: 11,193,207-11,361,163 LOC105371082, PRM1, 10 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
    nsv3910335copy number variation1nstd102humanLikely benign GRCh37 chr16: 10,872,408-11,468,030 , GRCh38 chr16: 10,778,551-11,374,173 , NCBI36 chr16: 10,779,909-11,375,531 HNRNPCP4, CIITA, 17 more genes
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