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 354

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7071971inversion1nstd229human GRCh38 chr18: 31,938,930-32,318,381 , GRCh37.p13 chr18: 29,518,893-29,898,344 TRAPPC8, RNA5SP453, 9 more genes
    nsv7071421inversion1nstd229human GRCh38 chr18: 31,321,802-32,119,916 , GRCh37.p13 chr18: 28,901,765-29,699,879 TTR, B4GALT6, 20 more genes
    nsv7070163inversion1nstd229human GRCh38 chr18: 31,760,869-32,125,867 , GRCh37.p13 chr18: 29,340,832-29,705,830 HMGN2P44, RNF138, 8 more genes
    nsv7068945inversion1nstd229human GRCh38 chr18: 32,110,424-32,113,776 , GRCh37.p13 chr18: 29,690,387-29,693,739 RNF138
    nsv7065049inversion1nstd229human GRCh38 chr18: 32,106,609-32,110,763 , GRCh37.p13 chr18: 29,686,572-29,690,726 RNF138
    nsv7059881inversion1nstd229human GRCh38 chr18: 31,754,105-32,126,675 , GRCh37.p13 chr18: 29,334,068-29,706,638 LOC100287539, PGDP1, 8 more genes
    nsv7012011copy number variation1nstd229human GRCh38 chr18: 32,019,864-32,123,267 , GRCh37.p13 chr18: 29,599,827-29,703,230 RNF138, HMGN2P44, 2 more genes
    nsv7011745copy number variation1nstd229human GRCh38 chr18: 32,086,517-32,098,372 , GRCh37.p13 chr18: 29,666,480-29,678,335 RNF125, RNF138
    nsv7010967copy number variation1nstd229human GRCh38 chr18: 32,095,398-32,095,994 , GRCh37.p13 chr18: 29,675,361-29,675,957 RNF138
    nsv7008256copy number variation1nstd229human GRCh38 chr18: 32,055,745-32,163,262 , GRCh37.p13 chr18: 29,635,708-29,743,225 RNF138, RPS15AP35, 1 more genes
    nsv7005726copy number variation1nstd229human GRCh38 chr18: 32,095,401-32,111,000 , GRCh37.p13 chr18: 29,675,364-29,690,963 RNF138
    nsv7004132copy number variation1nstd229human GRCh38 chr18: 32,102,013-32,104,131 , GRCh37.p13 chr18: 29,681,976-29,684,094 RNF138
    nsv7004076copy number variation1nstd229human GRCh38 chr18: 31,888,813-32,220,544 , GRCh37.p13 chr18: 29,468,776-29,800,507 TRAPPC8, RNU6-1050P, 9 more genes
    nsv7003751copy number variation1nstd229human GRCh38 chr18: 32,126,701-32,318,400 , GRCh37.p13 chr18: 29,706,664-29,898,363 GAREM1, RNF138, 3 more genes
    nsv7003015copy number variation1nstd229human GRCh38 chr18: 32,118,201-32,124,000 , GRCh37.p13 chr18: 29,698,164-29,703,963 RNF138
    nsv7002387copy number variation1nstd229human GRCh38 chr18: 32,117,717-32,123,192 , GRCh37.p13 chr18: 29,697,680-29,703,155 RNF138
    nsv7001778copy number variation1nstd229human GRCh38 chr18: 32,107,701-32,139,300 , GRCh37.p13 chr18: 29,687,664-29,719,263 RNF138
    nsv6998417copy number variation1nstd229human GRCh38 chr18: 32,126,248-32,126,454 , GRCh37.p13 chr18: 29,706,211-29,706,417 RNF138
    nsv6624551copy number variation3nstd224human GRCh37 chr18: 29,652,827-29,674,992 , GRCh38.p12 chr18: 32,072,864-32,095,029 RNF138, RNF125, 1 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center