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 81

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5209157copy number variation1nstd204human GRCh38.p13 chr1: 149,697,001-149,698,200 , GRCh37.p13 chr1|NW_003871055.3: 6,512,414-6,513,613 , GRCh37.p13 chr1: 149,668,548-149,669,787 RNU1-68P
    nsv5207916copy number variation1nstd204human GRCh37.p13 chr1|NW_003871055.3: 6,512,114-6,530,213 , GRCh37.p13 chr1: 149,668,248-149,686,338 , GRCh38.p13 chr1: 149,696,701-149,714,800 , LOC644634, 4 more genes
    nsv5207793copy number variation1nstd204human GRCh38.p13 chr1: 149,698,801-149,700,800 , GRCh37.p13 chr1|NW_003871055.3: 6,514,214-6,516,213 , GRCh37.p13 chr1: 149,670,380-149,672,372 , RNU1-68P, 1 more genes
    nsv5207015copy number variation1nstd204human GRCh38.p13 chr1: 149,696,601-149,699,300 , GRCh37.p13 chr1: 149,668,148-149,670,873 , GRCh37.p13 chr1|NW_003871055.3: 6,512,014-6,514,713 RNU1-68P
    nsv5206923copy number variation1nstd204human GRCh38.p13 chr1: 149,699,401-149,709,300 , GRCh37.p13 chr1: 149,670,974-149,680,845 , GRCh37.p13 chr1|NW_003871055.3: 6,514,814-6,524,713 , LOC100189498, 3 more genes
    nsv5205434copy number variation1nstd204human GRCh38.p13 chr1: 149,691,501-149,709,800 , GRCh37.p13 chr1|NW_003871055.3: 6,506,914-6,525,213 , GRCh37.p13 chr1: 149,663,052-149,681,348 , 3 more genes
    nsv5203528copy number variation1nstd204human GRCh38.p13 chr1: 149,691,501-149,701,400 , GRCh37.p13 chr1|NW_003871055.3: 6,506,914-6,516,813 , GRCh37.p13 chr1: 149,663,052-149,672,972 , RNU1-68P, 1 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv3963049copy number variation1nstd168human GRCh38 chr1: 148,246,304-149,713,197 , GRCh37.p13 chr1|NW_003871055.3: 5,061,717-6,528,610 , LINC02806, 57 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 , RNU1-153P, 4887 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , MARK1, 4930 more genes
    nsv3320413copy number variation1nstd162human GRCh38 chr1: 149,700,501-149,712,600 , GRCh37.p13 chr1: 149,672,073-149,684,147 , GRCh37.p13 chr1|NW_003871055.3: 6,515,914-6,528,013 , LOC644634, 4 more genes
    nsv3168056copy number variation1nstd158human GRCh38.p12 chr1: 84,243,714-179,997,709 , GRCh37 chr1: 84,709,397-179,966,844 , ABCA4, 1909 more genes
    nsv3167791inversion1nstd158human GRCh37 chr1: 42,414,066-227,813,903 , GRCh38.p12 chr1: 41,948,395-227,626,202 , ABCA4, 3418 more genes
    nsv1148209copy number variation1nstd107human GRCh37 chr1: 144,023,427-206,486,111 , GRCh38.p12 chr1: 120,324,463-206,312,767 , ABL2, 1659 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