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 212

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137668copy number variation1nstd102humannot provided GRCh37 chr18: 43,326,887-43,331,981 , GRCh38 chr18: 45,746,922-45,752,016 SLC14A1, LOC105372093
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5942602copy number variation1nstd209human GRCh38 chr18: 45,723,245-45,723,304 , GRCh37.p13 chr18: 43,303,210-43,303,269 SLC14A1, LOC105372092, 1 more genes
    nsv5935215copy number variation1nstd209human GRCh38 chr18: 45,730,165-45,731,771 , GRCh37.p13 chr18: 43,310,130-43,311,736 LOC105372093, SLC14A1
    nsv5929148copy number variation1nstd209human GRCh38 chr18: 45,741,755-45,741,828 , GRCh37.p13 chr18: 43,321,720-43,321,793 SLC14A1, LOC105372093
    nsv5878241copy number variation1nstd209human GRCh38 chr18: 45,730,218-45,731,717 , GRCh37.p13 chr18: 43,310,183-43,311,682 SLC14A1, LOC105372093
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv4676219copy number variation1nstd102humanPathogenic GRCh37 chr18: 41,630,585-45,107,905 , GRCh38.p12 chr18: 44,050,620-47,581,534 HAUS1, KATNAL2, 48 more genes
    nsv4676156copy number variation1nstd102humanPathogenic GRCh37 chr18: 39,800,804-44,365,152 , GRCh38.p12 chr18: 42,220,839-46,785,189 LOC105372089, RPS21P6, 40 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4530928copy number variation1nstd166human GRCh37.p13 chr18: 43,321,670-43,321,772 , GRCh38.p12 chr18: 45,741,705-45,741,807 SLC14A1, LOC105372093
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
    nsv3923838copy number variation1nstd102humanPathogenic NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381 WDR7-OT1, HMGN1P30, 941 more genes
    nsv3923800copy number variation1nstd102humanPathogenic GRCh38 chr18: 43,833,480-46,144,138 , GRCh37 chr18: 41,413,445-43,724,104 , NCBI36 chr18: 39,667,443-41,978,102 SETBP1, RN7SKP26, 27 more genes
    nsv3923799copy number variation1nstd102humanPathogenic GRCh38 chr18: 41,722,823-49,043,887 , GRCh37 chr18: 39,302,787-46,570,257 , NCBI36 chr18: 37,556,785-44,824,255 RNU6-1278P, RNA5SP454, 81 more genes
    nsv3921955copy number variation1nstd102humanPathogenic NCBI36 chr18: 38,169,137-42,560,421 , GRCh38 chr18: 42,335,174-46,726,460 , GRCh37 chr18: 39,915,139-44,306,423 ATP5F1A, LINC01478, 38 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