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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5528787copy number variation1nstd206human GRCh38 chr19: 34,757,099-34,757,615 , GRCh37.p13 chr19: 35,248,004-35,248,520 ZNF599
    nsv5359742translocation1nstd200human GRCh38 chr19: 34,757,099-34,757,099 , GRCh38 chr19: 34,757,615-34,757,615 , GRCh37.p13 chr19: 35,248,004-35,248,004 , GRCh37.p13 chr19: 35,248,520-35,248,520 ZNF599
    nsv5343263translocation1nstd200human GRCh37 chr19: 35,248,004-35,248,004 , GRCh37 chr19: 35,248,520-35,248,520 , GRCh38.p12 chr19: 34,757,615-34,757,615 , GRCh38.p12 chr19: 34,757,099-34,757,099 ZNF599
    nsv5020438copy number variation1nstd200human GRCh38 chr19: 34,771,120-34,771,269 , GRCh37.p13 chr19: 35,262,025-35,262,174 ZNF599
    nsv4665899copy number variation1nstd186human GRCh37 chr19: 35,248,003-35,248,520 , GRCh38.p12 chr19: 34,757,098-34,757,615 ZNF599
    nsv4628016copy number variation1nstd183human GRCh37 chr19: 35,248,003-35,248,520 , GRCh38.p12 chr19: 34,757,098-34,757,615 ZNF599
    nsv4564280mobile element insertion1nstd166human GRCh37.p13 chr19: 35,261,886-35,261,886 , GRCh38.p12 chr19: 34,770,981-34,770,981 ZNF599
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4421362copy number variation1nstd174human GRCh37 chr19: 35,247,982-35,248,520 , GRCh38.p12 chr19: 34,757,077-34,757,615 ZNF599
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4272300copy number variation1nstd166human GRCh37.p13 chr19: 35,247,854-35,248,520 , GRCh38.p12 chr19: 34,756,949-34,757,615 ZNF599
    nsv4269215copy number variation1nstd166human GRCh37.p13 chr19: 35,262,755-35,271,496 , GRCh38.p12 chr19: 34,771,850-34,780,592 ZNF599
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 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
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