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 164

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901938copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,746,094-76,780,189 , NCBI36 chrX: 76,632,750-76,666,845 , GRCh38 chrX: 77,490,616-77,524,711 ATRX
    nsv4451567copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,944,291-76,972,740 , GRCh38.p12 chrX: 77,688,798-77,717,263 ATRX
    nsv7098568copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,763,829-76,776,414 , GRCh38.p12 chrX: 77,508,351-77,520,936 ATRX
    nsv6634303copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,953,030-76,959,001 , GRCh38 chrX: 77,697,542-77,703,513 ATRX
    nsv5674118copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,937,002-76,940,508 , GRCh38.p12 chrX: 77,681,510-77,685,016 ATRX
    nsv6314704copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 76,940,499-76,972,607 , GRCh38.p12 chrX: 77,685,007-77,717,130 ATRX
    nsv7098569copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 76,937,002-76,972,730 , GRCh38.p12 chrX: 77,681,510-77,717,253 ATRX
    nsv6313466copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 76,953,051-76,954,137 , GRCh38.p12 chrX: 77,697,563-77,698,649 ATRX
    nsv3916560copy number variation1nstd102humanUncertain significance NCBI36 chrX: 76,900,154-76,917,451 , GRCh37.p13 chrX|NW_003871101.3: 315,279-332,575 , GRCh37.p13 chrX: 77,013,498-77,030,795 , GRCh38.p12 chrX: 77,758,017-77,775,313 ATRX
    nsv3914352copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,763,809-76,972,740 , GRCh38.p12 chrX: 77,508,331-77,717,263 ATRX
    nsv7098675copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,763,829-76,972,740 , GRCh38.p12 chrX: 77,508,351-77,717,263 ATRX
    nsv7093210copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,760,355-76,778,729 , GRCh38.p12 chrX: 77,504,877-77,523,251 ATRX
    nsv4681261copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,041,448-77,041,507 , GRCh38.p12 chrX: 77,785,962-77,786,021 ATRX
    nsv5674117copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,759,356-77,042,755 , GRCh38.p12 chrX: 77,503,878-77,787,277 ATRX, FABP5P15
    nsv997117copy number variation1nstd45humanPathogenic GRCh37 chrX: 76,760,356-77,041,755 , GRCh38.p12 chrX: 77,504,878-77,786,269 ATRX, FABP5P15
    nsv6313348copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 76,763,809-77,041,507 , GRCh38.p12 chrX: 77,508,331-77,786,021 ATRX, FABP5P15
    nsv3898440copy number variation1nstd102humanPathogenic NCBI36 chrX: 76,598,468-76,844,628 , GRCh37 chrX: 76,711,812-76,957,972 , GRCh38 chrX: 77,456,321-77,702,484 ATRX, FGF16
    nsv3871052copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,610,042-76,971,266 , GRCh38.p12 chrX: 77,389,579-77,715,775 ATRX, FGF16
    nsv6313465copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,759,357-77,042,755 , GRCh38.p12 chrX: 77,503,879-77,787,277 ATRX, FABP5P15
    nsv5381754copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,829,695-77,041,507 , GRCh38.p12 chrX: 77,574,230-77,786,021 ATRX, FABP5P15
    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