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 160

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 more genes
    nsv7054050inversion1nstd229human GRCh38 chr1: 160,407,483-160,413,041 , GRCh37.p13 chr1: 160,377,273-160,382,831 LOC105371466, VANGL2
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643127copy number variation1nstd229human GRCh38 chr1: 160,407,166-160,509,814 , GRCh37.p13 chr1: 160,376,956-160,479,604 SLAMF6, LOC105371466, 2 more genes
    nsv6642897copy number variation1nstd229human GRCh38 chr1: 160,297,601-160,434,000 , GRCh37.p13 chr1: 160,267,391-160,403,790 LOC105371466, VANGL2, 6 more genes
    nsv6637035copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,778,364-160,770,515 , GRCh38.p12 chr1: 159,808,574-160,800,725 PEX19, SLAMF8, 43 more genes
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6296170copy number variation1nstd186human GRCh37 chr1: 160,377,808-160,380,108 , GRCh38.p12 chr1: 160,408,018-160,410,318 VANGL2, LOC105371466
    nsv6133932copy number variation1nstd213human GRCh37 chr1: 160,280,000-160,600,001 , GRCh38.p12 chr1: 160,310,210-160,630,211 COPA, NCSTN, 10 more genes
    nsv6133931copy number variation1nstd213human GRCh37 chr1: 159,860,000-160,630,001 , GRCh38.p12 chr1: 159,890,210-160,660,211 COPA, NHLH1, 33 more genes
    nsv6133742copy number variation1nstd213human GRCh37 chr1: 158,430,000-161,510,001 , GRCh38.p12 chr1: 158,460,210-161,540,211 APCS, FCER1A, 174 more genes
    nsv6133741copy number variation1nstd213human GRCh37 chr1: 158,390,000-161,480,001 , GRCh38.p12 chr1: 158,420,210-161,510,211 ATP1A4, CD48, 169 more genes
    nsv6133740copy number variation1nstd213human GRCh37 chr1: 158,330,000-161,530,001 , GRCh38.p12 chr1: 158,360,210-161,560,211 ATP1A2, ATP1A4, 178 more genes
    nsv5562829sequence alteration1nstd206human GRCh38 chr1: 160,408,720-160,409,794 , GRCh37.p13 chr1: 160,378,510-160,379,584 VANGL2, LOC105371466
    nsv5556352inversion1nstd206human GRCh38 chr1: 160,408,705-160,409,814 , GRCh37.p13 chr1: 160,378,495-160,379,604 VANGL2, LOC105371466
    nsv5428736copy number variation1nstd206human GRCh38 chr1: 160,408,018-160,410,318 , GRCh37.p13 chr1: 160,377,808-160,380,108 LOC105371466, VANGL2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 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