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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5442408copy number variation1nstd206human GRCh38 chr2: 197,493,697-197,493,804 , GRCh37.p13 chr2: 198,358,421-198,358,528 HSPD1
    nsv5381571copy number variation1nstd102humanUncertain significance GRCh37 chr2: 198,351,760-198,363,582 , GRCh38.p12 chr2: 197,487,036-197,498,858 HSPE1, SNORA105B, 2 more genes
    nsv5180161mobile element insertion1nstd203human GRCh38 chr2: 197,485,010-197,485,019 , GRCh37.p13 chr2: 198,349,734-198,349,743 HSPD1, SNORA105B
    nsv5171331mobile element insertion1nstd203human GRCh38 chr2: 197,486,384-197,486,400 , GRCh37.p13 chr2: 198,351,108-198,351,124 HSPD1, SNORA105B
    nsv5079404mobile element insertion1nstd203human GRCh38 chr2: 197,495,621-197,495,645 , GRCh37.p13 chr2: 198,360,345-198,360,369 HSPD1
    nsv5073332mobile element insertion1nstd203human GRCh38 chr2: 197,495,623-197,495,645 , GRCh37.p13 chr2: 198,360,347-198,360,369 HSPD1
    nsv5070093mobile element insertion1nstd203human GRCh38 chr2: 197,495,614-197,495,645 , GRCh37.p13 chr2: 198,360,338-198,360,369 HSPD1
    nsv5068963mobile element insertion1nstd203human GRCh38 chr2: 197,495,595-197,495,645 , GRCh37.p13 chr2: 198,360,319-198,360,369 HSPD1
    nsv5067243mobile element insertion1nstd203human GRCh38 chr2: 197,495,617-197,495,645 , GRCh37.p13 chr2: 198,360,341-198,360,369 HSPD1
    nsv5063905mobile element insertion1nstd203human GRCh38 chr2: 197,495,609-197,495,645 , GRCh37.p13 chr2: 198,360,333-198,360,369 HSPD1
    nsv5061752mobile element insertion1nstd203human GRCh38 chr2: 197,495,645-197,495,677 , GRCh37.p13 chr2: 198,360,369-198,360,401 HSPD1
    nsv4913799copy number variation1nstd200human GRCh38 chr2: 197,487,307-197,518,619 , GRCh37.p13 chr2: 198,352,031-198,383,343 HSPE1-MOB4, HSPD1, 3 more genes
    nsv4910204copy number variation1nstd200human GRCh38 chr2: 197,499,074-197,502,543 , GRCh37.p13 chr2: 198,363,798-198,367,267 HSPD1, HSPE1-MOB4, 1 more genes
    nsv4795448copy number variation1nstd200human GRCh37 chr2: 198,363,798-198,367,267 , GRCh38.p12 chr2: 197,499,074-197,502,543 HSPE1, HSPE1-MOB4, 1 more genes
    nsv4768322copy number variation1nstd102humanPathogenic GRCh37 chr2: 197,359,024-201,383,462 , GRCh38.p12 chr2: 196,494,300-200,518,739 ANKRD44-DT, ATP5MC2P3, 48 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4727952copy number variation1nstd197human GRCh38.p12 chr2: 197,487,047-197,487,198 , GRCh37 chr2: 198,351,771-198,351,922 HSPD1, SNORA105B
    nsv4716529copy number variation1nstd102humanPathogenic GRCh37 chr2: 190,345,272-200,212,289 , GRCh38.p12 chr2: 189,480,546-199,347,566 C2orf66, LINC01821, 105 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
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