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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096621copy number variation1nstd102humanUncertain significance GRCh37 chr2: 236,403,331-237,032,766 , GRCh38.p12 chr2: 235,494,687-236,124,122 RN7SL204P, TMSB10P1, 5 more genes
    nsv7056978inversion1nstd229human GRCh38 chr2: 235,081,452-236,493,199 , GRCh37.p13 chr2: 235,990,096-237,401,842 LOC105373941, RNU7-127P, 14 more genes
    nsv6717089copy number variation1nstd229human GRCh38 chr2: 235,272,301-236,189,800 , GRCh37.p13 chr2: 236,180,945-237,098,443 LOC105373941, GBX2, 8 more genes
    nsv6716506copy number variation1nstd229human GRCh38 chr2: 235,472,001-235,619,500 , GRCh37.p13 chr2: 236,380,645-236,528,144 AGAP1-IT1, TNRC17, 1 more genes
    nsv6714166copy number variation1nstd229human GRCh38 chr2: 235,285,824-235,550,147 , GRCh37.p13 chr2: 236,194,468-236,458,791 LOC105373941, AGAP1-IT1, 2 more genes
    nsv6713303copy number variation1nstd229human GRCh38 chr2: 235,504,418-235,678,078 , GRCh37.p13 chr2: 236,413,062-236,586,722 AGAP1-IT1, TNRC17, 1 more genes
    nsv6711142copy number variation1nstd229human GRCh38 chr2: 234,674,418-235,726,282 , GRCh37.p13 chr2: 235,583,062-236,634,926 LOC105373939, LINC01173, 11 more genes
    nsv6710940copy number variation1nstd229human GRCh38 chr2: 235,084,015-235,524,155 , GRCh37.p13 chr2: 235,992,659-236,432,799 CEP19P1, AGAP1-IT1, 4 more genes
    nsv6709845copy number variation1nstd229human GRCh38 chr2: 235,503,107-235,519,244 , GRCh37.p13 chr2: 236,411,751-236,427,888 AGAP1-IT1, TNRC17, 1 more genes
    nsv6706138copy number variation1nstd229human GRCh38 chr2: 235,475,394-235,515,542 , GRCh37.p13 chr2: 236,384,038-236,424,186 AGAP1, AGAP1-IT1, 1 more genes
    nsv6705800copy number variation1nstd229human GRCh38 chr2: 235,490,071-235,530,717 , GRCh37.p13 chr2: 236,398,715-236,439,361 AGAP1-IT1, AGAP1, 1 more genes
    nsv6705720copy number variation1nstd229human GRCh38 chr2: 235,442,411-235,642,595 , GRCh37.p13 chr2: 236,351,055-236,551,239 AGAP1-IT1, AGAP1, 1 more genes
    nsv6702396copy number variation1nstd229human GRCh38 chr2: 235,494,501-236,404,300 , GRCh37.p13 chr2: 236,403,145-237,312,943 TMSB10P1, RNU1-31P, 10 more genes
    nsv6636912copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,642,145-237,654,870 , GRCh38.p12 chr2: 232,777,435-236,746,227 UGT1A, SH3BP4, 70 more genes
    nsv6636673copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,942,616-242,783,384 , GRCh38.p12 chr2: 235,033,972-241,841,232 LINC02991, OR6B3, 136 more genes
    nsv6352540copy number variation1nstd223human GRCh38 chr2: 235,361,091-235,669,534 , GRCh37.p13 chr2: 236,269,735-236,578,178 AGAP1-IT1, AGAP1, 2 more genes
    nsv6348858copy number variation1nstd223human GRCh38 chr2: 234,133,608-235,798,435 , GRCh37.p13 chr2: 235,042,252-236,707,079 LOC101927896, RPS20P12, 19 more genes
    nsv6347256copy number variation1nstd223human GRCh38 chr2: 234,674,418-235,726,282 , GRCh37.p13 chr2: 235,583,062-236,634,926 AGAP1, LOC105373940, 11 more genes
    nsv6340494copy number variation1nstd223human GRCh38 chr2: 235,326,054-235,677,919 , GRCh37.p13 chr2: 236,234,698-236,586,563 LOC105373941, AGAP1, 2 more genes
    nsv6339956copy number variation1nstd223human GRCh38 chr2: 235,503,801-235,519,100 , GRCh37.p13 chr2: 236,412,445-236,427,744 AGAP1-IT1, AGAP1, 1 more genes
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