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 226

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099225copy number variation1nstd231human GRCh38.p12 chr1: 111,381,594-114,553,029 , GRCh37 chr1: 111,924,216-115,095,650 ADORA3, RHOC, 74 more genes
    nsv7095695copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,145,905-114,454,813 , GRCh38.p12 chr1: 110,603,283-113,912,191 LOC107985189, RNU6-792P, 83 more genes
    nsv6640041copy number variation1nstd229human GRCh38 chr1: 111,386,455-111,403,140 , GRCh37.p13 chr1: 111,929,077-111,945,762 PGBP
    nsv6639948copy number variation1nstd229human GRCh38 chr1: 111,386,201-111,393,300 , GRCh37.p13 chr1: 111,928,823-111,935,922 PGBP
    nsv6639852copy number variation1nstd229human GRCh38 chr1: 111,386,206-111,392,204 , GRCh37.p13 chr1: 111,928,828-111,934,826 PGBP
    nsv6639851copy number variation1nstd229human GRCh38 chr1: 111,385,101-111,392,200 , GRCh37.p13 chr1: 111,927,723-111,934,822 PGBP
    nsv6639611copy number variation1nstd229human GRCh38 chr1: 111,386,401-111,393,400 , GRCh37.p13 chr1: 111,929,023-111,936,022 PGBP
    nsv6639609copy number variation1nstd229human GRCh38 chr1: 111,323,807-111,416,491 , GRCh37.p13 chr1: 111,866,429-111,959,113 OVGP1, CIMAP3, 4 more genes
    nsv6635742copy number variation2nstd227human GRCh37 chr1: 111,926,153-111,934,304 , GRCh38.p12 chr1: 111,383,531-111,391,682 PGBP
    nsv6634762copy number variation3nstd227human GRCh37 chr1: 111,929,295-111,934,304 , GRCh38.p12 chr1: 111,386,673-111,391,682 PGBP
    nsv6549317inversion1nstd223human GRCh38 chr1: 111,078,274-116,976,218 , GRCh37.p13 chr1: 111,620,896-117,518,840 RNU6-792P, TXNP3, 141 more genes
    nsv6318673copy number variation1nstd223human GRCh38 chr1: 111,386,201-111,392,200 , GRCh37.p13 chr1: 111,928,823-111,934,822 PGBP
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6133546copy number variation1nstd213human GRCh37 chr1: 111,330,000-112,310,001 , GRCh38.p12 chr1: 110,787,378-111,767,379 ADORA3, ATP5PB, 33 more genes
    nsv5880390copy number variation1nstd209human GRCh38 chr1: 111,386,205-111,392,201 , GRCh37.p13 chr1: 111,928,827-111,934,823 PGBP
    nsv5880056copy number variation1nstd209human GRCh38 chr1: 111,195,040-111,530,461 , GRCh37.p13 chr1: 111,737,662-112,073,083 , PGBP, 17 more genes
    nsv5827803copy number variation1nstd209human GRCh38 chr1: 111,385,463-111,392,143 , GRCh37.p13 chr1: 111,928,085-111,934,765 PGBP
    nsv5827802copy number variation1nstd209human GRCh38 chr1: 111,385,013-111,386,012 , GRCh37.p13 chr1: 111,927,635-111,928,634 PGBP
    nsv5673393copy number variation1nstd102humannot provided GRCh38 chr1: 111,383,529-111,391,680 , GRCh37 chr1: 111,926,151-111,934,302 PGBP
    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