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 296

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146242insertion1nstd232human GRCh37.p13 chr1: 207,001,477-207,001,477 , GRCh38.p12 chr1: 206,828,132-206,828,132 IL19
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7050697inversion1nstd229human GRCh38 chr1: 206,765,700-206,780,840 , GRCh37.p13 chr1: 206,940,870-206,954,185 IL19, IL10
    nsv7045682inversion1nstd229human GRCh38 chr1: 206,575,553-207,432,111 , GRCh37.p13 chr1: 206,940,870-207,605,456 CD55, RPS14P1, 26 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6676818copy number variation1nstd229human GRCh38 chr1: 206,831,182-206,833,726 , GRCh37.p13 chr1: 207,004,527-207,007,071 IL19
    nsv6668990copy number variation1nstd229human GRCh38 chr1: 206,823,642-206,826,977 , GRCh37.p13 chr1: 206,996,987-207,000,322 IL19
    nsv6667975copy number variation1nstd229human GRCh38 chr1: 206,808,652-206,812,903 , GRCh37.p13 chr1: 206,981,997-206,986,248 IL19
    nsv6664547copy number variation1nstd229human GRCh38 chr1: 206,825,501-206,832,700 , GRCh37.p13 chr1: 206,998,846-207,006,045 IL19
    nsv6661741copy number variation1nstd229human GRCh38 chr1: 206,831,074-206,841,824 , GRCh37.p13 chr1: 207,004,419-207,015,169 IL19, LOC105372878
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6626152copy number variation1nstd224human GRCh37 chr1: 207,015,957-207,040,730 , GRCh38.p12 chr1: 206,842,612-206,867,385 IL19, IL20, 1 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6549406inversion1nstd223human GRCh38 chr1: 206,775,066-206,776,927 , GRCh37.p13 chr1: 206,948,411-206,950,272 IL19
    nsv6332004copy number variation1nstd223human GRCh38 chr1: 206,809,399-206,813,997 , GRCh37.p13 chr1: 206,982,744-206,987,342 IL19
    nsv6329625copy number variation1nstd223human GRCh38 chr1: 206,784,094-206,785,554 , GRCh37.p13 chr1: 206,957,439-206,958,899 IL19
    nsv6310745copy number variation2nstd102humanUncertain significance GRCh37 chr1: 206,941,981-208,391,267 , GRCh38.p12 chr1: 206,768,636-208,217,922 PFKFB2, LOC105372878, 39 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