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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943179copy number variation1nstd209human GRCh38 chr19: 46,837,556-46,837,722 , GRCh37.p13 chr19: 47,340,813-47,340,979 AP2S1
    nsv5933330copy number variation1nstd209human GRCh38 chr19: 46,835,407-46,837,257 , GRCh37.p13 chr19: 47,338,664-47,340,514 AP2S1
    nsv5883555copy number variation1nstd209human GRCh38 chr19: 46,835,338-46,837,337 , GRCh37.p13 chr19: 47,338,595-47,340,594 AP2S1
    nsv5528219copy number variation1nstd206human GRCh38 chr19: 46,835,431-46,837,258 , GRCh37.p13 chr19: 47,338,688-47,340,515 AP2S1
    nsv5173746mobile element insertion1nstd203human GRCh38 chr19: 46,848,379-46,848,394 , GRCh37.p13 chr19: 47,351,636-47,351,651 AP2S1
    nsv5024750copy number variation1nstd200human GRCh38 chr19: 46,841,535-46,912,344 , GRCh37.p13 chr19: 47,344,792-47,415,601 ARHGAP35, AP2S1
    nsv5024749copy number variation1nstd200human GRCh38 chr19: 46,832,735-46,839,217 , GRCh37.p13 chr19: 47,335,992-47,342,474 AP2S1
    nsv5024745copy number variation1nstd200human GRCh38 chr19: 46,758,373-46,850,779 , GRCh37.p13 chr19: 47,261,630-47,354,036 , SLC1A5, 4 more genes
    nsv5020793copy number variation1nstd200human GRCh38 chr19: 46,835,431-46,837,258 , GRCh37.p13 chr19: 47,338,688-47,340,515 AP2S1
    nsv4907556mobile element deletion1nstd200human GRCh38 chr19: 46,843,441-46,843,731 , GRCh37.p13 chr19: 47,346,698-47,346,988 AP2S1
    nsv4865221copy number variation1nstd200human GRCh37 chr19: 47,335,992-47,342,474 , GRCh38.p12 chr19: 46,832,735-46,839,217 AP2S1
    nsv4853158copy number variation1nstd200human GRCh37 chr19: 47,338,688-47,340,515 , GRCh38.p12 chr19: 46,835,431-46,837,258 AP2S1
    nsv4775432mobile element deletion1nstd200human GRCh37 chr19: 47,346,698-47,346,988 , GRCh38.p12 chr19: 46,843,441-46,843,731 AP2S1
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4676254copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,331,662-48,234,260 , GRCh38.p12 chr19: 46,828,405-47,731,003 AP2S1, BICRA, 22 more genes
    nsv4673715copy number variation1nstd186human GRCh37 chr19: 47,338,665-47,340,518 , GRCh38.p12 chr19: 46,835,408-46,837,261 AP2S1
    nsv4666099copy number variation1nstd186human GRCh37 chr19: 47,339,060-47,340,263 , GRCh38.p12 chr19: 46,835,803-46,837,006 AP2S1
    nsv4623334copy number variation1nstd183human GRCh37 chr19: 47,338,665-47,340,518 , GRCh38.p12 chr19: 46,835,408-46,837,261 AP2S1
    nsv4620760copy number variation2nstd183human GRCh37 chr19: 47,339,060-47,340,263 , GRCh38.p12 chr19: 46,835,803-46,837,006 AP2S1
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