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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682037copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310 XAB2, CLEC4G, 40 more genes
    nsv4676269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878 LRRC8E, CLEC4GP1, 47 more genes
    nsv4629101copy number variation1nstd183human GRCh37 chr19: 7,397,015-7,925,985 , GRCh38.p12 chr19: 7,332,094-7,861,099 , PEX11G, 27 more genes
    nsv4257097copy number variation1nstd166human GRCh37.p13 chr19: 7,786,000-7,836,900 , GRCh38.p12 chr19: 7,721,114-7,772,014 CLEC4M, CD209, 4 more genes
    nsv3968684copy number variation1nstd168human GRCh38 chr19: 7,709,461-7,727,455 , GRCh37.p13 chr19: 7,774,347-7,792,341 CLEC4G
    nsv3917314copy number variation1nstd102humanUncertain significance NCBI36 chr19: 7,145,928-7,798,318 , GRCh38 chr19: 7,194,917-7,827,432 , GRCh37 chr19: 7,194,928-7,892,318 CLEC4G, STXBP2, 26 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
    nsv3911630copy number variation1nstd102humanLikely benign GRCh37 chr19: 7,787,972-7,948,153 , GRCh38 chr19: 7,723,086-7,883,268 , NCBI36 chr19: 7,693,972-7,854,153 CLEC4M, CD209, 9 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3892807copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,747,084-7,793,833 , GRCh38.p12 chr19: 7,682,198-7,728,947 TRAPPC5, CLEC4G, 2 more genes
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 PCP2, EIF1P6, 250 more genes
    nsv3165763copy number variation1nstd151human GRCh37 chr19: 7,504,825-8,155,140 , GRCh38.p12 chr19: 7,439,939-8,090,256 SAXO5, LYPLA2P2, 39 more genes
    nsv3164705copy number variation1nstd151human GRCh37 chr19: 7,794,023-7,828,367 , GRCh38.p12 chr19: 7,729,137-7,763,481 RPL21P129, CD209, 3 more genes
    nsv3162975copy number variation1nstd151human GRCh37 chr19: 7,794,704-7,833,879 , GRCh38.p12 chr19: 7,729,818-7,768,993 CD209, CLEC4G, 4 more genes
    nsv3160254copy number variation1nstd151human GRCh37 chr19: 7,764,622-7,965,803 , GRCh38.p12 chr19: 7,699,736-7,900,918 EVI5L, CD209, 13 more genes
    nsv2768220copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 5,092,438-17,933,476 , GRCh37 chr19: 5,092,449-18,044,285 , ACP5, 562 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-20,692,745 , GRCh37 chr19: 260,911-20,875,551 , ACP5, 914 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-19,745,645 , GRCh37 chr19: 260,911-19,856,454 , ACP5, 867 more genes
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