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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5937483copy number variation1nstd209human GRCh38 chr16: 57,628,892-57,629,035 , GRCh37.p13 chr16: 57,662,804-57,662,947 ADGRG1
    nsv5672929copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,693,297-57,697,504 , GRCh38.p12 chr16: 57,659,385-57,663,592 ADGRG1, ADGRG3
    nsv5599767copy number variation1nstd207human GRCh38 chr16: 57,628,889-57,628,940 , GRCh37.p13 chr16: 57,662,801-57,662,852 ADGRG1
    nsv5309282copy number variation1nstd204human GRCh38.p13 chr16: 57,584,497-57,694,311 , GRCh37.p13 chr16: 57,618,409-57,728,223 ADGRG1, DRC7, 4 more genes
    nsv5275681copy number variation1nstd204human GRCh38.p13 chr16: 57,641,421-57,642,748 , GRCh37.p13 chr16: 57,675,333-57,676,660 ADGRG1
    nsv5272366copy number variation1nstd204human GRCh38.p13 chr16: 57,658,264-57,659,613 , GRCh37.p13 chr16: 57,692,176-57,693,525 ADGRG1
    nsv5270649copy number variation1nstd204human GRCh37.p13 chr16: 57,618,413-57,728,212 , GRCh38.p13 chr16: 57,584,501-57,694,300 ADGRG1, DRC7, 4 more genes
    nsv5263827copy number variation1nstd204human GRCh38.p13 chr16: 57,586,711-57,670,453 , GRCh37.p13 chr16: 57,620,623-57,704,365 ADGRG3, HMGB3P32, 3 more genes
    nsv5262379copy number variation1nstd204human GRCh38.p13 chr16: 57,632,254-57,633,353 , GRCh37.p13 chr16: 57,666,166-57,667,265 ADGRG1
    nsv5261573copy number variation1nstd204human GRCh38.p13 chr16: 57,650,322-57,652,323 , GRCh37.p13 chr16: 57,684,234-57,686,235 ADGRG1
    nsv5261273copy number variation1nstd204human GRCh38.p13 chr16: 57,643,324-57,646,405 , GRCh37.p13 chr16: 57,677,236-57,680,317 ADGRG1
    nsv5008404copy number variation1nstd200human GRCh38 chr16: 57,662,166-57,662,695 , GRCh37.p13 chr16: 57,696,078-57,696,607 ADGRG3, ADGRG1
    nsv5005705copy number variation1nstd200human GRCh38 chr16: 57,617,356-57,618,756 , GRCh37.p13 chr16: 57,651,268-57,652,668 ADGRG1
    nsv4857219copy number variation1nstd200human GRCh37 chr16: 57,696,078-57,696,607 , GRCh38.p12 chr16: 57,662,166-57,662,695 ADGRG3, ADGRG1
    nsv4857217copy number variation1nstd200human GRCh37 chr16: 57,618,432-57,728,202 , GRCh38.p12 chr16: 57,584,520-57,694,290 ADGRG1, DRC7, 4 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729888copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,292,407-59,103,985 , GRCh38.p12 chr16: 57,258,495-59,070,081 HMGB3P32, DOK4, 57 more genes
    nsv4683790copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,689,301-57,694,798 , GRCh38.p12 chr16: 57,655,389-57,660,886 ADGRG1
    nsv4681796copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,689,301-57,697,504 , GRCh38.p12 chr16: 57,655,389-57,663,592 ADGRG1, ADGRG3
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