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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935065copy number variation1nstd209human GRCh38 chr19: 7,867,960-7,868,257 , GRCh37.p13 chr19: 7,932,846-7,933,143 PRR36
    nsv5587345copy number variation1nstd207human GRCh38 chr19: 7,870,908-7,870,976 , GRCh37.p13 chr19: 7,935,794-7,935,862 PRR36
    nsv5525292copy number variation1nstd206human GRCh38 chr19: 7,874,812-7,876,626 , GRCh37.p13 chr19: 7,939,697-7,941,511 PRR36, LYPLA2P2
    nsv4743332copy number variation1nstd199human GRCh37 chr19: 7,935,801-7,935,869 , GRCh38.p12 chr19: 7,870,915-7,870,983 PRR36
    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
    nsv4670534copy number variation1nstd186human GRCh37 chr19: 7,934,682-7,936,047 , GRCh38.p12 chr19: 7,869,796-7,871,161 PRR36
    nsv4633210copy number variation2nstd183human GRCh37 chr19: 7,934,682-7,936,047 , GRCh38.p12 chr19: 7,869,796-7,871,161 PRR36
    nsv4623166copy number variation1nstd183human GRCh37 chr19: 7,934,890-7,936,855 , GRCh38.p12 chr19: 7,870,004-7,871,969 PRR36
    nsv4439813copy number variation1nstd175human GRCh37 chr19: 7,935,794-7,935,863 , GRCh38.p12 chr19: 7,870,908-7,870,977 PRR36
    nsv4424773copy number variation1nstd174human GRCh37 chr19: 7,935,848-7,935,947 , GRCh38.p12 chr19: 7,870,962-7,871,061 PRR36
    nsv4414264copy number variation1nstd174human GRCh37 chr19: 7,935,437-7,936,546 , GRCh38.p12 chr19: 7,870,551-7,871,660 PRR36
    nsv3956041copy number variation1nstd168human GRCh38 chr19: 7,859,413-7,901,845 , GRCh37.p13 chr19: 7,924,299-7,966,730 MAP2K7, LRRC8E, 4 more genes
    nsv3931053copy number variation1nstd167human GRCh37 chr19: 7,935,794-7,935,863 , GRCh38.p12 chr19: 7,870,908-7,870,977 PRR36
    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
    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
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