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 455

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073159inversion1nstd229human GRCh38 chr19: 249,047-1,189,238 , GRCh37.p13 chr19: 249,047-1,189,237 MADCAM1-AS1, ARID3A, 53 more genes
    nsv7063137inversion1nstd229human GRCh38 chr19: 363,262-504,084 , GRCh37.p13 chr19: 363,262-504,084 SHC2, SPMAP2, 5 more genes
    nsv7058460inversion1nstd229human GRCh38 chr19: 322,195-777,239 , GRCh37.p13 chr19: 322,195-777,239 PRSS57, RPS2P52, 23 more genes
    nsv7009236copy number variation1nstd229human GRCh38 chr19: 479,569-506,294 , GRCh37.p13 chr19: 479,569-506,294 MADCAM1-AS1, CIMAP1D, 2 more genes
    nsv7008358copy number variation1nstd229human GRCh38 chr19: 376,752-507,545 , GRCh37.p13 chr19: 376,752-507,545 SHC2, RNA5SP462, 6 more genes
    nsv7006585copy number variation1nstd229human GRCh38 chr19: 387,915-576,682 , GRCh37.p13 chr19: 387,915-576,682 CDC34, C2CD4C, 9 more genes
    nsv6637450copy number variation1nstd102humanUncertain significance GRCh37 chr19: 260,912-508,202 , GRCh38.p12 chr19: 260,912-508,202 VN2R11P, C2CD4C, 9 more genes
    nsv6637255copy number variation1nstd102humanUncertain significance GRCh37 chr19: 260,912-538,303 , GRCh38.p12 chr19: 260,912-538,303 C2CD4C, CDC34, 10 more genes
    nsv6625217copy number variation2nstd224human GRCh37 chr19: 474,588-521,076 , GRCh38.p12 chr19: 474,588-521,076 MADCAM1, TPGS1, 2 more genes
    nsv6625216copy number variation1nstd224human GRCh37 chr19: 467,706-511,453 , GRCh38.p12 chr19: 467,706-511,453 CIMAP1D, TPGS1, 2 more genes
    nsv6625163copy number variation1nstd224human GRCh37 chr19: 483,488-518,884 , GRCh38.p12 chr19: 483,488-518,884 MADCAM1, TPGS1, 2 more genes
    nsv6625162copy number variation1nstd224human GRCh37 chr19: 474,588-504,948 , GRCh38.p12 chr19: 474,588-504,948 MADCAM1-AS1, MADCAM1, 1 more genes
    nsv6625030copy number variation1nstd224human GRCh37 chr19: 487,375-517,315 , GRCh38.p12 chr19: 487,375-517,315 CIMAP1D, TPGS1, 2 more genes
    nsv6625028copy number variation1nstd224human GRCh37 chr19: 482,984-511,453 , GRCh38.p12 chr19: 482,984-511,453 TPGS1, MADCAM1-AS1, 2 more genes
    nsv6625025copy number variation1nstd224human GRCh37 chr19: 474,588-517,315 , GRCh38.p12 chr19: 474,588-517,315 CIMAP1D, MADCAM1, 2 more genes
    nsv6625024copy number variation27nstd224human GRCh37 chr19: 474,588-511,453 , GRCh38.p12 chr19: 474,588-511,453 MADCAM1, MADCAM1-AS1, 2 more genes
    nsv6625022copy number variation1nstd224human GRCh37 chr19: 470,796-521,076 , GRCh38.p12 chr19: 470,796-521,076 MADCAM1, MADCAM1-AS1, 2 more genes
    nsv6625021copy number variation1nstd224human GRCh37 chr19: 464,207-504,948 , GRCh38.p12 chr19: 464,207-504,948 CIMAP1D, MADCAM1-AS1, 1 more genes
    nsv6624895copy number variation1nstd224human GRCh37 chr19: 388,413-606,473 , GRCh38.p12 chr19: 388,413-606,473 BSG-AS1, HCN2, 11 more genes
    nsv6624773copy number variation1nstd224human GRCh37 chr19: 483,488-521,076 , GRCh38.p12 chr19: 483,488-521,076 CIMAP1D, MADCAM1-AS1, 2 more genes
    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