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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5832964copy number variation1nstd209human GRCh38 chr2: 3,564,731-3,574,542 , GRCh37.p13 chr2: 3,612,321-3,622,132 RPS7
    nsv5381250copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,622,941-3,628,472 , GRCh38.p12 chr2: 3,575,351-3,580,882 RPS7
    nsv4904716copy number variation1nstd200human GRCh38 chr2: 3,577,005-3,577,504 , GRCh37.p13 chr2: 3,624,595-3,625,094 RPS7
    nsv4904711copy number variation1nstd200human GRCh38 chr2: 3,358,584-3,733,756 , GRCh37.p13 chr2: 3,362,355-3,781,346 RNASEH1, TRAPPC12, 11 more genes
    nsv4728726copy number variation1nstd102humanUncertain significance GRCh37 chr2: 2,529,149-5,511,339 , GRCh38.p12 chr2: 2,525,377-5,371,206 LOC107985840, COLEC11, 24 more genes
    nsv4728695copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,385,474-4,974,948 , GRCh38.p12 chr2: 3,381,703-4,927,358 LOC105373397, LOC105373394, 17 more genes
    nsv4728621copy number variation1nstd102humanPathogenic GRCh37 chr2: 2,074,335-3,934,366 , GRCh38.p12 chr2: 2,070,563-3,886,776 LOC105373389, MYT1L, 18 more genes
    nsv4674784copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,045,542-4,104,255 , GRCh38.p12 chr2: 1,049,856-4,056,664 LOC105373390, MYT1L-AS1, 27 more genes
    nsv4454966copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665 LINC01810, ADI1, 83 more genes
    nsv4452632copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-3,819,558 , GRCh38.p12 chr2: 12,770-3,771,968 LOC107985838, LOC100996637, 45 more genes
    nsv4057543copy number variation1nstd166human GRCh37.p13 chr2: 3,362,355-3,781,346 , GRCh38.p12 chr2: 3,358,584-3,733,756 ADI1, COLEC11, 11 more genes
    nsv4057431copy number variation1nstd166human GRCh37.p13 chr2: 3,615,374-3,621,632 , GRCh38.p12 chr2: 3,567,784-3,574,042 RPS7
    nsv3908677copy number variation1nstd102humanUncertain significance NCBI36 chr2: 2,770-4,344,326 , GRCh37 chr2: 12,770-4,366,451 , GRCh38 chr2: 12,770-4,318,861 LINC01865, EIPR1, 50 more genes
    nsv3908628copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951 RPS7, RPL30P3, 198 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3908459copy number variation1nstd102humanPathogenic NCBI36 chr2: 1,647,394-23,740,517 , GRCh38 chr2: 1,664,615-23,664,142 , GRCh37 chr2: 1,668,387-23,887,012 EIF1P7, LOC105373398, 277 more genes
    nsv3908405copy number variation1nstd102humanPathogenic GRCh38 chr2: 17,019-20,001,056 , NCBI36 chr2: 7,019-20,064,298 , GRCh37 chr2: 17,019-20,200,817 LOC100996549, LOC105373479, 252 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 ALLC, LOC105373429, 674 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 LOC105373394, PGAM1P6, 507 more genes
    nsv3907033copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531 GTF3C2-AS1, LOC105373399, 434 more genes
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