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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5440393copy number variation1nstd206human GRCh38 chr2: 10,067,065-10,070,546 , GRCh37.p13 chr2: 10,207,192-10,210,673 CYS1
    nsv5207879copy number variation1nstd204human GRCh38.p13 chr2: 10,060,680-10,062,879 , GRCh37.p13 chr2: 10,200,807-10,203,006 CYS1
    nsv4904756copy number variation1nstd200human GRCh38 chr2: 10,010,915-10,140,233 , GRCh37.p13 chr2: 10,151,042-10,280,360 , RRM2, 4 more genes
    nsv4892298copy number variation1nstd200human GRCh38 chr2: 10,067,077-10,072,098 , GRCh37.p13 chr2: 10,207,204-10,212,225 CYS1
    nsv4892297copy number variation1nstd200human GRCh38 chr2: 10,061,809-10,061,933 , GRCh37.p13 chr2: 10,201,936-10,202,060 CYS1
    nsv4892296copy number variation1nstd200human GRCh38 chr2: 10,060,397-10,063,808 , GRCh37.p13 chr2: 10,200,524-10,203,935 CYS1
    nsv4537156insertion1nstd166human GRCh37.p13 chr2: 10,203,643-10,203,643 , GRCh38.p12 chr2: 10,063,516-10,063,516 CYS1
    nsv4071341copy number variation1nstd166human GRCh37.p13 chr2: 10,200,524-10,203,935 , GRCh38.p12 chr2: 10,060,397-10,063,808 CYS1
    nsv3908896copy number variation1nstd102humanPathogenic GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372 RNU6-1288P, MIR7515HG, 138 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
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3896997copy number variation1nstd102humanPathogenic GRCh38 chr2: 12,770-25,039,694 , GRCh37 chr2: 12,770-25,262,563 , NCBI36 chr2: 2,770-25,116,067 LOC105373359, MYT1L-AS1, 333 more genes
    nsv3893260copy number variation1nstd102humanPathogenic GRCh37 chr2: 17,019-26,541,714 , GRCh38 chr2: 17,019-26,318,846 , NCBI36 chr2: 7,019-26,395,218 LOC102723389, LOC105373433, 362 more genes
    nsv3887944copy number variation1nstd102humanUncertain significance GRCh37 chr2: 10,192,688-10,462,223 , GRCh38.p12 chr2: 10,052,561-10,322,097 CYS1, LOC101929691, 6 more genes
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