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Items: 1 to 20 of 106

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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
    nsv5940892copy number variation1nstd209human GRCh38 chr19: 6,375,477-6,388,120 , GRCh37.p13 chr19: 6,375,488-6,388,131 GTF2F1, ALKBH7, 2 more genes
    nsv5882330copy number variation1nstd209human GRCh38 chr19: 6,374,432-6,384,823 , GRCh37.p13 chr19: 6,374,443-6,384,834 GTF2F1, PSPN, 1 more genes
    nsv5531245copy number variation1nstd206human GRCh38 chr19: 6,370,513-6,370,988 , GRCh37.p13 chr19: 6,370,524-6,370,999 CLPP, ALKBH7
    nsv5320977copy number variation1nstd204human GRCh38.p13 chr19: 6,375,453-6,388,144 , GRCh37.p13 chr19: 6,375,464-6,388,155 MIR6885, ALKBH7, 2 more genes
    nsv5292311copy number variation1nstd204human GRCh38.p13 chr19: 6,374,201-6,489,700 , GRCh37.p13 chr19: 6,374,212-6,489,711 GTF2F1, SLC25A41, 10 more genes
    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
    nsv5027477copy number variation1nstd200human GRCh38 chr19: 6,358,630-6,389,172 , GRCh37.p13 chr19: 6,358,641-6,389,183 GTF2F1, PSPN, 4 more genes
    nsv5014430copy number variation1nstd200human GRCh38 chr19: 6,375,477-6,388,121 , GRCh37.p13 chr19: 6,375,488-6,388,132 GTF2F1, PSPN, 2 more genes
    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
    nsv4671143copy number variation1nstd186human GRCh37 chr19: 6,374,916-6,389,245 , GRCh38.p12 chr19: 6,374,905-6,389,234 GTF2F1, PSPN, 2 more genes
    nsv4627187copy number variation1nstd183human GRCh37 chr19: 6,375,673-6,381,199 , GRCh38.p12 chr19: 6,375,662-6,381,188 PSPN, GTF2F1, 1 more genes
    nsv4623394copy number variation1nstd183human GRCh37 chr19: 6,374,916-6,389,245 , GRCh38.p12 chr19: 6,374,905-6,389,234 ALKBH7, GTF2F1, 2 more genes
    nsv4262012copy number variation1nstd166human GRCh37.p13 chr19: 6,373,134-6,373,197 , GRCh38.p12 chr19: 6,373,123-6,373,186 PSPN, ALKBH7
    nsv4260460copy number variation1nstd166human GRCh37.p13 chr19: 6,375,488-6,388,132 , GRCh38.p12 chr19: 6,375,477-6,388,121 MIR6885, ALKBH7, 2 more genes
    nsv4259986copy number variation1nstd166human GRCh37.p13 chr19: 6,370,394-6,370,999 , GRCh38.p12 chr19: 6,370,383-6,370,988 ALKBH7, CLPP
    nsv3966173insertion1nstd168human GRCh38 chr19: 6,360,305-6,381,599 , GRCh37.p13 chr19: 6,360,316-6,381,610 GTF2F1, PSPN, 3 more genes
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