U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 31

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4450313copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,508,782-38,587,992 , GRCh38.p12 chr2: 38,281,640-38,360,850 ATL2, GAPDHP25
    nsv4450643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,509,406-38,587,992 , GRCh38.p12 chr2: 38,282,264-38,360,850 ATL2, GAPDHP25
    nsv4453591copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,510,607-38,587,992 , GRCh38.p12 chr2: 38,283,465-38,360,850 ATL2, GAPDHP25
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 ATL2, CYP1B1-AS1, 1649 more genes
    nsv6313619copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300 ATL2, LOC107985870, 161 more genes
    nsv3899050copy number variation1nstd102humanPathogenic NCBI36 chr2: 37,081,204-42,035,330 , GRCh37 chr2: 37,227,700-42,181,826 , GRCh38 chr2: 37,000,557-41,954,686 ATL2, LOC375196, 78 more genes
    nsv7096503copy number variation1nstd102humanPathogenic GRCh37 chr2: 38,297,865-38,917,056 , GRCh38.p12 chr2: 38,070,722-38,689,914 ATL2, CYP1B1, 13 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 ATL2, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 ATL2, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 ATL2, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 ATL2, MTND2P22, 3724 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 ATL2, SLC35F6, 801 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 ATL2, ALLC, 674 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 ATL2, RPL7P13, 426 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 ATL2, UBXN2A, 465 more genes
    nsv3882842copy number variation1nstd102humanPathogenic GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406 ATL2, STON1, 303 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 ATL2, GTF3C2-AS1, 316 more genes
    nsv3877469copy number variation1nstd102humanPathogenic GRCh37 chr2: 28,069,882-43,543,420 , GRCh38.p12 chr2: 27,847,015-43,316,281 ATL2, FOSL2, 219 more genes
    nsv7096652copy number variation1nstd102humanPathogenic GRCh37 chr2: 37,334,416-39,347,563 , GRCh38.p12 chr2: 37,107,273-39,120,422 ATL2, RPL31P16, 52 more genes
    nsv3911681inversion1nstd102humanPathogenic GRCh38.p12 chr2: 29,223,528-42,325,554 , GRCh37 chr2: 29,446,394-42,552,694 ATL2, ALK, 163 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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