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Items: 1 to 20 of 22261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137663copy number variation1nstd102humannot provided GRCh38 chr2: 46,009,609-46,144,092 , GRCh37.p13 chr2: 46,236,748-46,371,231 PRKCE
    nsv6131352insertion1nstd186human GRCh37 chr17: 43,991,589-43,991,622 , GRCh38.p12 chr17|NT_187663.1: 616,338-616,371 , GRCh38.p12 chr17: 45,914,223-45,914,256 MAPT
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130841insertion1nstd186human GRCh37 chr19: 3,145,581-3,145,581 , GRCh38.p12 chr19: 3,145,583-3,145,583 GNA15-DT, GNA15
    nsv6130729mobile element insertion1nstd186human GRCh37 chr5: 159,351,199-159,351,250 , GRCh38.p12 chr5: 159,924,192-159,924,243 ADRA1B
    nsv6130532insertion1nstd186human GRCh37 chr16: 56,377,254-56,377,290 , GRCh38.p12 chr16: 56,343,342-56,343,378 GNAO1
    nsv6129462insertion1nstd186human GRCh37 chr14: 24,794,428-24,794,428 , GRCh38.p12 chr14: 24,325,222-24,325,222 , GRCh38.p12 chr14|NW_018654722.1: 626,200-626,200 ADCY4
    nsv6129269insertion1nstd186human GRCh37 chr14: 52,427,349-52,427,369 , GRCh38.p12 chr14: 51,960,631-51,960,651 GNG2
    nsv6124828insertion1nstd186human GRCh37 chr8: 141,960,170-141,960,193 , GRCh38.p12 chr8: 140,950,071-140,950,094 PTK2
    nsv6124825insertion1nstd186human GRCh37 chr5: 7,704,113-7,704,113 , GRCh38.p12 chr5: 7,704,000-7,704,000 ADCY2
    nsv6121886copy number variation1nstd186human GRCh37 chr14: 52,393,881-52,393,974 , GRCh38.p12 chr14: 51,927,163-51,927,256 GNG2
    nsv6121122copy number variation1nstd186human GRCh37 chr14: 52,404,345-52,404,457 , GRCh38.p12 chr14: 51,937,627-51,937,739 GNG2
    nsv6117446mobile element insertion1nstd186human GRCh37 chr21: 32,784,221-32,784,221 , GRCh38.p12 chr21: 31,411,908-31,411,908 TIAM1
    nsv6115984mobile element insertion1nstd186human GRCh37 chr14: 30,044,324-30,044,335 , GRCh38.p12 chr14: 29,575,118-29,575,129 PRKD1
    nsv6115904mobile element insertion1nstd186human GRCh37 chr16: 4,097,485-4,097,536 , GRCh38.p12 chr16: 4,047,484-4,047,535 ADCY9
    nsv6113132mobile element insertion1nstd186human GRCh37 chr21: 32,633,420-32,633,445 , GRCh38.p12 chr21: 31,261,104-31,261,129 LOC105372777, TIAM1
    nsv6112910mobile element insertion1nstd186human GRCh37 chr16: 4,086,447-4,086,498 , GRCh38.p12 chr16: 4,036,446-4,036,497 ADCY9
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
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