U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 107

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112733copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735 LOC112267888, LOC105373454, 40 more genes
    nsv5440197copy number variation1nstd206human GRCh38 chr2: 17,750,919-18,037,345 , GRCh37.p13 chr2: 17,932,186-18,218,611 KCNS3, SMC6, 5 more genes
    nsv5288740copy number variation1nstd204human GRCh38.p13 chr2: 17,706,276-18,478,642 , GRCh37.p13 chr2: 17,887,543-18,659,908 KCNS3, SMC6, 7 more genes
    nsv5215060copy number variation1nstd204human GRCh37.p13 chr2: 17,887,568-18,659,766 , GRCh38.p13 chr2: 17,706,301-18,478,500 KCNS3, SMC6, 7 more genes
    nsv4904814copy number variation1nstd200human GRCh38 chr2: 17,750,919-18,037,345 , GRCh37.p13 chr2: 17,932,186-18,218,611 MSGN1, LOC105373449, 5 more genes
    nsv4788298copy number variation1nstd200human GRCh37 chr2: 17,932,186-18,218,611 , GRCh38.p12 chr2: 17,750,919-18,037,345 KCNS3, SMC6, 5 more genes
    nsv4728764copy number variation1nstd102humanUncertain significance GRCh37 chr2: 17,846,161-18,720,906 , GRCh38.p12 chr2: 17,664,894-18,539,640 MSGN1, SMC6, 7 more genes
    nsv4595121copy number variation1nstd183human GRCh37 chr2: 17,341,974-18,336,233 , GRCh38.p12 chr2: 17,160,707-18,154,967 KCNS3, LOC105373449, 12 more genes
    nsv4451073copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,269,293-18,259,781 , GRCh38.p12 chr2: 12,129,167-18,078,515 LINC00276, TRIB2, 49 more genes
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 82 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
    nsv3891917copy number variation1nstd102humanPathogenic GRCh37 chr2: 16,904,863-21,823,606 , GRCh38 chr2: 16,723,596-21,600,734 , NCBI36 chr2: 16,768,344-21,677,111 LOC105373454, RAD51AP2, 68 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center