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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5906535copy number variation1nstd209human GRCh38 chr5: 36,192,649-36,192,702 , GRCh37.p13 chr5: 36,192,751-36,192,804 NADK2
    nsv5903129copy number variation1nstd209human GRCh38 chr5: 36,193,216-36,193,403 , GRCh37.p13 chr5: 36,193,318-36,193,505 NADK2
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5313622copy number variation1nstd204human GRCh38.p13 chr5: 36,215,024-36,216,371 , GRCh37.p13 chr5: 36,215,126-36,216,473 NADK2
    nsv5233458copy number variation1nstd204human GRCh38.p13 chr5: 36,215,001-36,216,400 , GRCh37.p13 chr5: 36,215,103-36,216,502 NADK2
    nsv4946654copy number variation1nstd200human GRCh38 chr5: 36,234,589-36,237,893 , GRCh37.p13 chr5: 36,234,691-36,237,995 NADK2
    nsv4946653copy number variation1nstd200human GRCh38 chr5: 36,215,028-36,216,370 , GRCh37.p13 chr5: 36,215,130-36,216,472 NADK2
    nsv4946652copy number variation1nstd200human GRCh38 chr5: 36,203,746-36,205,681 , GRCh37.p13 chr5: 36,203,848-36,205,783 NADK2
    nsv4944598copy number variation1nstd200human GRCh38 chr5: 36,208,588-36,298,488 , GRCh37.p13 chr5: 36,208,690-36,298,590 RANBP3L, NADK2
    nsv4805394copy number variation1nstd200human GRCh37 chr5: 36,208,690-36,298,590 , GRCh38.p12 chr5: 36,208,588-36,298,488 NADK2, RANBP3L
    nsv4802515copy number variation1nstd200human GRCh37 chr5: 36,215,130-36,216,470 , GRCh38.p12 chr5: 36,215,028-36,216,368 NADK2
    nsv4802514copy number variation1nstd200human GRCh37 chr5: 36,203,858-36,205,779 , GRCh38.p12 chr5: 36,203,756-36,205,677 NADK2
    nsv4598089copy number variation1nstd183human GRCh37 chr5: 36,203,658-36,315,463 , GRCh38.p12 chr5: 36,203,556-36,315,361 RANBP3L, NADK2
    nsv4598088copy number variation1nstd183human GRCh37 chr5: 36,201,331-36,318,595 , GRCh38.p12 chr5: 36,201,229-36,318,493 RANBP3L, NADK2
    nsv4571842mobile element insertion1nstd166human GRCh37.p13 chr5: 36,225,810-36,225,810 , GRCh38.p12 chr5: 36,225,708-36,225,708 NADK2
    nsv4571170mobile element insertion1nstd166human GRCh37.p13 chr5: 36,204,239-36,204,239 , GRCh38.p12 chr5: 36,204,137-36,204,137 NADK2
    nsv4570661mobile element insertion1nstd166human GRCh37.p13 chr5: 36,239,249-36,239,249 , GRCh38.p12 chr5: 36,239,147-36,239,147 NADK2
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
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