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 96

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147729insertion1nstd232human GRCh37.p13 chr1: 24,022,398-24,022,398 , GRCh38.p12 chr1: 23,695,908-23,695,908 RPL11
    nsv7140339insertion1nstd232human GRCh37.p13 chr1: 24,020,408-24,020,408 , GRCh38.p12 chr1: 23,693,918-23,693,918 RPL11
    nsv7099186copy number variation1nstd231human GRCh38.p12 chr1: 23,507,765-23,861,716 , GRCh37 chr1: 23,834,257-24,188,206 E2F2, FUCA1, 15 more genes
    nsv7095983copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,021,140-24,022,863 , GRCh38.p12 chr1: 23,694,650-23,696,373 RPL11
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7093236copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,022,350-24,022,761 , GRCh38 chr1: 23,695,860-23,696,271 RPL11
    nsv7045385inversion1nstd229human GRCh38 chr1: 23,660,402-23,737,189 , GRCh37.p13 chr1: 23,986,892-24,063,679 RPL11, EEF1A1P48
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv7041183inversion1nstd229human GRCh38 chr1: 23,625,460-23,891,463 , GRCh37.p13 chr1: 23,951,950-24,217,953 CNR2, HMGCL, 11 more genes
    nsv7039758inversion1nstd229human GRCh38 chr1: 23,654,445-23,737,485 , GRCh37.p13 chr1: 23,980,935-24,063,975 RPL11, EEF1A1P48
    nsv6647427copy number variation1nstd229human GRCh38 chr1: 23,690,481-23,690,512 , GRCh37.p13 chr1: 24,016,971-24,017,002 RPL11
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6636547copy number variation1nstd102humanPathogenic GRCh37 chr1: 23,980,892-24,024,498 , GRCh38.p12 chr1: 23,654,402-23,698,008 EEF1A1P48, RPL11
    nsv6636481copy number variation1nstd102humanUncertain significance GRCh37 chr1: 23,680,995-24,224,241 , GRCh38.p12 chr1: 23,354,502-23,897,751 CNR2, E2F2, 20 more genes
    nsv6315455copy number variation1nstd102humanPathogenic GRCh37 chr1: 23,814,543-24,163,928 , GRCh38.p12 chr1: 23,488,050-23,837,438 LOC105376860, LOC101928163, 14 more genes
    nsv6290023insertion1nstd102humanPathogenic GRCh37 chr1: 24,021,276-24,021,276 , GRCh38 chr1: 23,694,786-23,694,786 RPL11
    nsv6133987copy number variation1nstd213human GRCh37 chr1: 24,010,000-24,370,001 , GRCh38.p12 chr1: 23,683,510-24,043,511 CNR2, FUCA1, 17 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 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