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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076231inversion1nstd229human GRCh38 chr17: 69,015,631-73,552,061 , GRCh37.p13 chr17: 67,011,772-71,548,200 KCNJ2-AS1, ROCR, 52 more genes
    nsv7063183inversion1nstd229human GRCh38 chr17: 68,931,960-70,066,756 , GRCh37.p13 chr17: 66,928,101-68,062,897 LOC105371878, ABCA8, 18 more genes
    nsv6996184copy number variation1nstd229human GRCh38 chr17: 69,893,135-70,001,422 , GRCh37.p13 chr17: 67,889,276-67,997,563 LINC01497, LOC105371881, 1 more genes
    nsv6996024copy number variation1nstd229human GRCh38 chr17: 69,961,543-69,961,942 , GRCh37.p13 chr17: 67,957,684-67,958,083 LINC01497
    nsv6995773copy number variation1nstd229human GRCh38 chr17: 69,979,788-70,043,170 , GRCh37.p13 chr17: 67,975,929-68,039,311 LOC112267896, LINC01497, 1 more genes
    nsv6993014copy number variation1nstd229human GRCh38 chr17: 69,963,901-69,967,200 , GRCh37.p13 chr17: 67,960,042-67,963,341 LINC01497
    nsv6991112copy number variation1nstd229human GRCh38 chr17: 69,968,594-69,971,594 , GRCh37.p13 chr17: 67,964,735-67,967,735 LINC01497
    nsv6984301copy number variation1nstd229human GRCh38 chr17: 69,893,135-69,964,853 , GRCh37.p13 chr17: 67,889,276-67,960,994 LINC01483, LINC01497
    nsv6978197copy number variation1nstd229human GRCh38 chr17: 69,979,501-70,006,500 , GRCh37.p13 chr17: 67,975,642-68,002,641 LOC105371881, LINC01497
    nsv6638043copy number variation1nstd102humanUncertain significance GRCh37 chr17: 67,730,594-68,272,354 , GRCh38.p12 chr17: 69,734,453-70,276,213 LINC01483, KCNJ2, 8 more genes
    nsv6535518copy number variation1nstd223human GRCh38 chr17: 69,962,001-69,963,500 , GRCh37.p13 chr17: 67,958,142-67,959,641 LINC01497
    nsv6533757copy number variation1nstd223human GRCh38 chr17: 69,969,376-69,970,525 , GRCh37.p13 chr17: 67,965,517-67,966,666 LINC01497
    nsv6530697copy number variation1nstd223human GRCh38 chr17: 69,977,880-69,986,291 , GRCh37.p13 chr17: 67,974,021-67,982,432 LINC01497
    nsv6529628copy number variation1nstd223human GRCh38 chr17: 69,961,543-69,961,942 , GRCh37.p13 chr17: 67,957,684-67,958,083 LINC01497
    nsv6522513copy number variation1nstd223human GRCh38 chr17: 69,982,501-69,986,409 , GRCh37.p13 chr17: 67,978,642-67,982,550 LINC01497
    nsv6521020copy number variation1nstd223human GRCh38 chr17: 69,974,691-69,975,661 , GRCh37.p13 chr17: 67,970,832-67,971,802 LINC01497
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv6081392insertion1nstd212human GRCh38 chr17: 69,961,629-69,961,629 , GRCh37.p13 chr17: 67,957,770-67,957,770 LINC01497
    nsv6026050copy number variation1nstd212human GRCh38 chr17: 69,961,545-69,961,942 , GRCh37.p13 chr17: 67,957,686-67,958,083 LINC01497
    nsv5702232mobile element insertion2nstd211human GRCh38 chr17: 69,972,933-69,972,933 , GRCh37.p13 chr17: 67,969,074-67,969,074 LINC01497
    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