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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5874880copy number variation1nstd209human GRCh38 chr19: 6,582,021-6,583,146 , GRCh37.p13 chr19: 6,582,032-6,583,157 CD70
    nsv5523181copy number variation1nstd206human GRCh38 chr19: 6,579,308-6,582,092 , GRCh37.p13 chr19: 6,579,319-6,582,103 CD70
    nsv5320484copy number variation1nstd204human GRCh38.p13 chr19: 6,590,688-6,590,971 , GRCh37.p13 chr19: 6,590,699-6,590,982 CD70
    nsv5285813copy number variation1nstd204human GRCh38.p13 chr19: 5,731,901-6,700,600 , GRCh37.p13 chr19: 5,731,912-6,700,611 MIR6885, LOC390877, 38 more genes
    nsv5179283mobile element insertion1nstd203human GRCh38 chr19: 6,591,538-6,591,582 , GRCh37.p13 chr19: 6,591,549-6,591,593 CD70, RPL7P50
    nsv4852783copy number variation1nstd200human GRCh37 chr19: 6,587,190-6,587,511 , GRCh38.p12 chr19: 6,587,179-6,587,500 CD70
    nsv4729892copy number variation1nstd102humanUncertain significance GRCh37 chr19: 6,096,399-6,699,729 , GRCh38.p12 chr19: 6,096,388-6,699,718 TUBB4A, KHSRP, 24 more genes
    nsv4676363copy number variation1nstd102humanUncertain significance GRCh37 chr19: 6,246,138-6,823,741 , GRCh38.p12 chr19: 6,246,127-6,823,730 SLC25A23, PSPN, 26 more genes
    nsv4676137copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,949,772-6,699,729 , GRCh38.p12 chr19: 5,949,761-6,699,718 MIR6885, LOC390877, 27 more genes
    nsv4265558copy number variation1nstd166human GRCh37.p13 chr19: 6,580,731-6,581,355 , GRCh38.p12 chr19: 6,580,720-6,581,344 CD70
    nsv3956839copy number variation1nstd168human GRCh38 chr19: 6,505,290-6,654,462 , GRCh37.p13 chr19: 6,505,301-6,654,473 RPL7P50, CLIC4P2, 3 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3918411copy number variation1nstd102humanUncertain significance GRCh38 chr19: 5,905,175-6,916,287 , GRCh37 chr19: 5,905,186-6,916,298 , NCBI36 chr19: 5,856,186-6,867,298 CAPS, MIR6790, 36 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
    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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