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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125806copy number variation1nstd186human GRCh37 chr19: 35,513,553-35,513,603 , GRCh38.p12 chr19: 35,022,649-35,022,699 GRAMD1A
    nsv5971329insertion1nstd209human GRCh38 chr19: 35,022,695-35,022,695 , GRCh37.p13 chr19: 35,513,599-35,513,599 GRAMD1A
    nsv5650988insertion1nstd207human GRCh38 chr19: 35,022,695-35,022,695 , GRCh37.p13 chr19: 35,513,599-35,513,599 GRAMD1A
    nsv5517313copy number variation1nstd206human GRCh38 chr19: 35,022,649-35,022,699 , GRCh37.p13 chr19: 35,513,553-35,513,603 GRAMD1A
    nsv5517120copy number variation1nstd206human GRCh38 chr19: 34,998,582-35,001,841 , GRCh37.p13 chr19: 35,489,486-35,492,745 GRAMD1A
    nsv5027684copy number variation1nstd200human GRCh38 chr19: 35,003,413-35,003,520 , GRCh37.p13 chr19: 35,494,317-35,494,424 GRAMD1A
    nsv5027683copy number variation1nstd200human GRCh38 chr19: 34,988,927-35,002,592 , GRCh37.p13 chr19: 35,479,831-35,493,496 GRAMD1A
    nsv4765780insertion1nstd199human GRCh37 chr19: 35,513,589-35,513,589 , GRCh38.p12 chr19: 35,022,685-35,022,685 GRAMD1A
    nsv4726528insertion1nstd186human GRCh37 chr19: 35,513,553-35,513,553 , GRCh38.p12 chr19: 35,022,649-35,022,649 GRAMD1A
    nsv4545093insertion1nstd166human GRCh37.p13 chr19: 35,513,553-35,513,553 , GRCh38.p12 chr19: 35,022,649-35,022,649 GRAMD1A
    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
    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
    nsv4268224copy number variation1nstd166human GRCh37.p13 chr19: 35,494,317-35,494,424 , GRCh38.p12 chr19: 35,003,413-35,003,520 GRAMD1A
    nsv4264365copy number variation1nstd166human GRCh37.p13 chr19: 35,507,748-35,507,883 , GRCh38.p12 chr19: 35,016,844-35,016,979 GRAMD1A
    nsv4253200copy number variation1nstd166human GRCh37.p13 chr19: 35,515,301-35,515,404 , GRCh38.p12 chr19: 35,024,397-35,024,500 GRAMD1A
    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
    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
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