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 130

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965504insertion1nstd209human GRCh38 chr1: 119,510,711-119,510,711 , GRCh37.p13 chr1: 120,053,334-120,053,334 HSD3B1
    nsv5563805sequence alteration1nstd206human GRCh38 chr1: 119,513,952-119,514,186 , GRCh37.p13 chr1: 120,056,575-120,056,809 HSD3B1
    nsv5079506mobile element insertion1nstd203human GRCh38 chr1: 119,510,717-119,510,754 , GRCh37.p13 chr1: 120,053,340-120,053,377 HSD3B1
    nsv5063585mobile element insertion1nstd203human GRCh38 chr1: 119,505,953-119,505,999 , GRCh37.p13 chr1: 120,048,576-120,048,622 HSD3B1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4673945copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,836,834-120,289,623 , GRCh38.p12 chr1: 119,294,211-119,747,000 GAPDHP58, HSD3BP2, 21 more genes
    nsv4453677copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,425,395-120,527,495 , GRCh38.p12 chr1: 118,882,772-119,984,872 HSD3B2, GAPDHP23, 36 more genes
    nsv4411458copy number variation1nstd174human GRCh37 chr1: 119,847,447-120,154,798 , GRCh38.p12 chr1: 119,304,824-119,612,175 HSD3B1, HSD3BP4, 17 more genes
    nsv3902952copy number variation1nstd102humanUncertain significance NCBI36 chr1: 119,278,003-120,321,801 , GRCh38 chr1: 118,933,857-119,977,655 , GRCh37 chr1: 119,476,480-120,471,049 NBPF7P, LOC105378933, 36 more genes
    nsv3902511copy number variation1nstd102humanPathogenic NCBI36 chr1: 116,403,765-120,474,160 , GRCh38 chr1: 116,059,621-120,130,051 , GRCh37 chr1: 116,602,242-120,672,637 LINC01779, REG4, 89 more genes
    nsv3891366copy number variation1nstd102humanLikely benign NCBI36 chr1: 119,096,385-120,321,742 , GRCh38 chr1: 118,752,239-119,977,596 , GRCh37 chr1: 119,294,862-120,520,219 HSD3BP2, LOC105378933, 37 more genes
    nsv3890331copy number variation1nstd102humanPathogenic NCBI36 chr1: 104,669,629-120,321,801 , GRCh37 chr1: 104,868,106-120,471,049 , GRCh38 chr1: 104,325,484-119,977,655 OR11I1P, NHLH2, 324 more genes
    nsv3885279copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,806,427-120,438,201 , GRCh38.p12 chr1: 119,263,804-119,895,578 HSD3BP1, GAPDHP33, 27 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
    nsv3882464copy number variation1nstd102humanPathogenic GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985 LINC02607, RNVU1-19, 513 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , MARK1, 4930 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