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 173

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6642113copy number variation1nstd229human GRCh38 chr1: 150,993,923-150,998,604 , GRCh37.p13 chr1: 150,966,399-150,971,080 ANXA9, MINDY1
    nsv6641779copy number variation1nstd229human GRCh38 chr1: 150,994,122-150,998,846 , GRCh37.p13 chr1: 150,966,598-150,971,322 ANXA9, MINDY1
    nsv6641778copy number variation1nstd229human GRCh38 chr1: 150,981,286-150,985,858 , GRCh37.p13 chr1: 150,953,762-150,958,334 ANXA9, LOC105371438
    nsv6641777copy number variation1nstd229human GRCh38 chr1: 150,967,801-151,307,200 , GRCh37.p13 chr1: 150,940,277-151,279,676 MINDY1, TNFAIP8L2, 23 more genes
    nsv6641764copy number variation1nstd229human GRCh38 chr1: 150,761,787-151,277,656 , GRCh37.p13 chr1: 150,734,263-151,250,132 VPS72, RPS29P29, 30 more genes
    nsv6625395copy number variation1nstd224human GRCh37 chr1: 150,951,477-151,011,437 , GRCh38.p12 chr1: 150,979,001-151,038,961 ANXA9, MINDY1, 4 more genes
    nsv6546546inversion1nstd223human GRCh38 chr1: 150,990,380-150,991,503 , GRCh37.p13 chr1: 150,962,856-150,963,979 ANXA9
    nsv6325186copy number variation1nstd223human GRCh38 chr1: 150,994,972-150,996,281 , GRCh37.p13 chr1: 150,967,448-150,968,757 MINDY1, ANXA9
    nsv6322457copy number variation1nstd223human GRCh38 chr1: 150,980,726-150,991,426 , GRCh37.p13 chr1: 150,953,202-150,963,902 ANXA9, LOC105371438
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133733copy number variation1nstd213human GRCh37 chr1: 149,980,000-151,620,001 , GRCh38.p12 chr1: 150,008,051-151,647,525 CTSK, MCL1, 80 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv6055008insertion1nstd212human GRCh38 chr1: 150,990,242-150,990,242 , GRCh37.p13 chr1: 150,962,718-150,962,718 ANXA9
    nsv5962444insertion1nstd209human GRCh38 chr1: 150,990,242-150,990,242 , GRCh37.p13 chr1: 150,962,718-150,962,718 ANXA9
    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