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 27

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095758copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,142,597-156,146,788 , GRCh38.p12 chr1: 156,172,806-156,176,997 SEMA4A
    nsv7095483copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,130,214-156,132,905 , GRCh38.p12 chr1: 156,160,423-156,163,114 SEMA4A
    nsv3885968copy number variation1nstd102humanPathogenic GRCh37 chr1: 156,070,888-156,238,593 , GRCh38.p12 chr1: 156,101,097-156,268,802 SEMA4A, BGLAP, 6 more genes
    nsv4450954copy number variation1nstd102humanPathogenic GRCh37 chr1: 156,084,710-156,212,953 , GRCh38 chr1: 156,114,919-156,243,162 SEMA4A, BGLAP, 5 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 SEMA4A, CRB1, 1608 more genes
    nsv3882925copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,636,337-158,024,499 , GRCh38.p12 chr1: 155,666,546-158,054,709 SEMA4A, SH2D2A, 88 more genes
    nsv6310593copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,581,953-156,851,434 , GRCh38.p12 chr1: 155,612,162-156,881,642 SEMA4A, MIR9-1, 62 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 SEMA4A, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 SEMA4A, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 SEMA4A, RNU1-153P, 4887 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 SEMA4A, LOC101060227, 1608 more genes
    nsv3900459copy number variation1nstd102humanPathogenic GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332 SEMA4A, HORMAD1, 923 more genes
    nsv3917016copy number variation1nstd102humanPathogenic NCBI36 chr1: 152,220,775-155,340,341 , GRCh37.p13 chr1: 153,954,151-157,073,717 , GRCh38.p12 chr1: 153,981,675-157,103,925 SEMA4A, SMU1P1, 152 more genes
    nsv3906950copy number variation1nstd102humanPathogenic GRCh38 chr1: 154,566,501-157,624,084 , NCBI36 chr1: 152,805,601-155,860,498 , GRCh37 chr1: 154,538,977-157,593,874 SEMA4A, ARHGEF2-AS2, 131 more genes
    nsv3870644copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 153,751,465-156,660,462 , GRCh38.p12 chr1: 153,778,989-156,690,670 SEMA4A, ADAR, 145 more genes
    nsv3909898inversion1nstd102humanLikely pathogenic GRCh38.p12 chr1: 154,158,509-156,874,085 , GRCh37 chr1: 154,130,985-156,843,877 SEMA4A, ADAR, 136 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 SEMA4A, DCST1, 2428 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 SEMA4A, PRPF3, 352 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 SEMA4A, MIR555, 135 more genes
    nsv4452342copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,770,505-156,652,136 , GRCh38.p12 chr1: 155,800,714-156,682,344 SEMA4A, NES, 43 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