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 332

    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
    nsv7095696copy number variation1nstd102humanPathogenic GRCh37 chr1: 112,318,699-115,576,848 , GRCh38.p12 chr1: 111,776,077-115,034,227 AKR7A2P1, PTPN22, 69 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
    nsv7053817inversion1nstd229human GRCh38 chr1: 112,472,093-113,188,421 , GRCh37.p13 chr1: 113,014,715-113,731,043 LOC107985189, NUTF2P4, 22 more genes
    nsv7047135inversion1nstd229human GRCh38 chr1: 112,389,397-113,355,432 , GRCh37.p13 chr1: 112,932,019-113,898,054 LRIG2-DT, PPM1J, 26 more genes
    nsv7046226inversion1nstd229human GRCh38 chr1: 112,507,311-113,213,376 , GRCh37.p13 chr1: 113,049,933-113,755,998 NUTF2P4, LINC01357, 24 more genes
    nsv6640084copy number variation1nstd229human GRCh38 chr1: 112,526,683-112,534,019 , GRCh37.p13 chr1: 113,069,305-113,076,641 WNT2B, ST7L
    nsv6640082copy number variation1nstd229human GRCh38 chr1: 112,498,065-112,664,236 , GRCh37.p13 chr1: 113,040,687-113,206,858 CAPZA1, MRPL53P1, 3 more genes
    nsv6640081copy number variation1nstd229human GRCh38 chr1: 112,490,913-112,518,758 , GRCh37.p13 chr1: 113,033,535-113,061,380 ST7L, WNT2B
    nsv6639985copy number variation1nstd229human GRCh38 chr1: 112,494,080-112,495,297 , GRCh37.p13 chr1: 113,036,702-113,037,919 WNT2B
    nsv6639984copy number variation1nstd229human GRCh38 chr1: 112,478,706-112,479,463 , GRCh37.p13 chr1: 113,021,328-113,022,085 WNT2B
    nsv6639876copy number variation1nstd229human GRCh38 chr1: 112,505,747-112,518,232 , GRCh37.p13 chr1: 113,048,369-113,060,854 WNT2B, ST7L
    nsv6639874copy number variation1nstd229human GRCh38 chr1: 112,460,324-112,465,207 , GRCh37.p13 chr1: 113,002,946-113,007,829 WNT2B, MIR4256, 1 more genes
    nsv6636643copy number variation1nstd102humanUncertain significance GRCh37 chr1: 112,680,493-113,047,932 , GRCh38.p12 chr1: 112,137,871-112,505,310 MIR4256, TXNP3, 3 more genes
    nsv6551028inversion1nstd223human GRCh38 chr1: 112,473,807-112,474,276 , GRCh37.p13 chr1: 113,016,429-113,016,898 WNT2B
    nsv6549317inversion1nstd223human GRCh38 chr1: 111,078,274-116,976,218 , GRCh37.p13 chr1: 111,620,896-117,518,840 RNU6-792P, TXNP3, 141 more genes
    nsv6549200inversion1nstd223human GRCh38 chr1: 112,498,246-112,498,973 , GRCh37.p13 chr1: 113,040,868-113,041,595 WNT2B
    nsv6546492inversion1nstd223human GRCh38 chr1: 112,479,116-112,479,726 , GRCh37.p13 chr1: 113,021,738-113,022,348 WNT2B
    nsv6543963inversion1nstd223human GRCh38 chr1: 112,488,060-112,488,854 , GRCh37.p13 chr1: 113,030,682-113,031,476 WNT2B
    nsv6540679inversion1nstd223human GRCh38 chr1: 112,479,729-112,480,387 , GRCh37.p13 chr1: 113,022,351-113,023,009 WNT2B
    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