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 522

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096576copy number variation1nstd102humanPathogenic GRCh37 chr2: 166,237,583-166,246,334 , GRCh38.p12 chr2: 165,381,073-165,389,824 SCN2A
    nsv7096575copy number variation1nstd102humanUncertain significance GRCh37 chr2: 166,018,798-166,246,334 , GRCh38.p12 chr2: 165,162,288-165,389,824 SCN2A, MAPRE1P3, 1 more genes
    nsv7096574copy number variation1nstd102humanPathogenic GRCh37 chr2: 165,946,660-167,108,415 , GRCh38.p12 chr2: 165,090,150-166,251,905 SCN3A, MAPRE1P3, 11 more genes
    nsv7096377copy number variation1nstd102humanPathogenic GRCh37 chr2: 166,237,651-166,240,529 , GRCh38.p12 chr2: 165,381,141-165,384,019 SCN2A
    nsv7096376copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 166,237,239-166,239,066 , GRCh38.p12 chr2: 165,380,729-165,382,556 SCN2A
    nsv7096375copy number variation1nstd102humanUncertain significance GRCh37 chr2: 166,226,616-166,226,829 , GRCh38.p12 chr2: 165,370,106-165,370,319 SCN2A
    nsv7096374copy number variation1nstd102humanUncertain significance GRCh37 chr2: 165,984,121-166,246,334 , GRCh38.p12 chr2: 165,127,611-165,389,824 MAPRE1P3, SCN3A, 1 more genes
    nsv7096373copy number variation1nstd102humanUncertain significance GRCh37 chr2: 165,946,660-166,894,662 , GRCh38.p12 chr2: 165,090,150-166,038,152 TTC21B, SCN3A, 8 more genes
    nsv7045559inversion1nstd229human GRCh38 chr2: 165,384,670-165,384,682 , GRCh37.p13 chr2: 166,241,180-166,241,192 SCN2A
    nsv7041761inversion1nstd229human GRCh38 chr2: 161,208,254-165,696,625 , GRCh37.p13 chr2: 162,064,765-166,553,135 SCN3A, LOC101929532, 45 more genes
    nsv7039563inversion1nstd229human GRCh38 chr2: 165,267,302-165,271,229 , GRCh37.p13 chr2: 166,123,812-166,127,739 SCN2A
    nsv7039552inversion1nstd229human GRCh38 chr2: 161,275,467-165,696,611 , GRCh37.p13 chr2: 162,131,978-166,553,121 LOC105373722, EIF3EP3, 42 more genes
    nsv6695873copy number variation1nstd229human GRCh38 chr2: 165,232,801-165,243,000 , GRCh37.p13 chr2: 166,089,311-166,099,510 SCN2A
    nsv6689984copy number variation1nstd229human GRCh38 chr2: 165,253,701-165,259,300 , GRCh37.p13 chr2: 166,110,211-166,115,810 SCN2A
    nsv6689189copy number variation1nstd229human GRCh38 chr2: 165,316,190-165,316,644 , GRCh37.p13 chr2: 166,172,700-166,173,154 SCN2A
    nsv6685018copy number variation1nstd229human GRCh38 chr2: 165,223,470-165,223,576 , GRCh37.p13 chr2: 166,079,980-166,080,086 SCN2A
    nsv6681520copy number variation1nstd229human GRCh38 chr2: 165,320,302-165,320,326 , GRCh37.p13 chr2: 166,176,812-166,176,836 SCN2A
    nsv6680178copy number variation1nstd229human GRCh38 chr2: 165,302,301-165,304,600 , GRCh37.p13 chr2: 166,158,811-166,161,110 SCN2A
    nsv6554514inversion1nstd223human GRCh38 chr2: 165,338,265-165,339,242 , GRCh37.p13 chr2: 166,194,775-166,195,752 SCN2A
    nsv6545731inversion1nstd223human GRCh38 chr2: 165,260,110-165,260,797 , GRCh37.p13 chr2: 166,116,620-166,117,307 SCN2A
    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