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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142204copy number variation1nstd232human GRCh37.p13 chr16: 1,010,371-1,010,461 , GRCh38.p12 chr16: 960,371-960,461 LMF1
    nsv7141988copy number variation1nstd232human GRCh37.p13 chr16: 1,003,952-1,004,061 , GRCh38.p12 chr16: 953,952-954,061 LMF1
    nsv7138842insertion1nstd232human GRCh37.p13 chr16: 969,548-969,548 , GRCh38.p12 chr16: 919,548-919,548 LMF1, LMF1-AS1
    nsv7137545copy number variation1nstd232human GRCh37.p13 chr16: 980,073-980,131 , GRCh38.p12 chr16: 930,073-930,131 LMF1, LMF1-AS1
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 more genes
    nsv7094951copy number variation1nstd102humanPathogenic GRCh37 chr16: 960,911-961,099 , GRCh38.p12 chr16: 910,911-911,099 LMF1
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7094663copy number variation2nstd102humanPathogenic GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266 TPSP2, PRR25, 83 more genes
    nsv7094645copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,004,337-1,004,686 , GRCh38.p12 chr16: 954,337-954,686 LMF1
    nsv7077616inversion1nstd229human GRCh38 chr16: 875,410-906,005 , GRCh37.p13 chr16: 925,410-956,005 LOC107984876, LMF1
    nsv7073654inversion1nstd229human GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907 UBE2I, CRAMP1, 45 more genes
    nsv6977519copy number variation1nstd229human GRCh38 chr16: 966,601-972,500 , GRCh37.p13 chr16: 1,016,601-1,022,500 LMF1
    nsv6977243copy number variation1nstd229human GRCh38 chr16: 930,102-933,180 , GRCh37.p13 chr16: 980,102-983,180 LMF1-AS1, LMF1
    nsv6977134copy number variation1nstd229human GRCh38 chr16: 951,401-1,472,200 , GRCh37.p13 chr16: 1,001,401-1,522,201 TPSG1, TPSAB1, 27 more genes
    nsv6975809copy number variation1nstd229human GRCh38 chr16: 864,201-869,200 , GRCh37.p13 chr16: 914,201-919,200 LMF1
    nsv6975503copy number variation1nstd229human GRCh38 chr16: 874,760-881,268 , GRCh37.p13 chr16: 924,760-931,268 LMF1
    nsv6975468copy number variation1nstd229human GRCh38 chr16: 959,029-975,724 , GRCh37.p13 chr16: 1,009,029-1,025,724 CEROX1, LMF1
    nsv6974692copy number variation1nstd229human GRCh38 chr16: 864,749-865,474 , GRCh37.p13 chr16: 914,749-915,474 LMF1
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