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 122

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098914copy number variation1nstd102humanUncertain significance GRCh38 chr9: 68,417,620-68,744,894 , GRCh37.p13 chr9: 71,130,848-71,359,810 PGM5, TMEM252-DT, 5 more genes
    nsv6875533copy number variation1nstd229human GRCh38 chr9: 68,543,501-68,549,400 , GRCh37.p13 chr9: 71,158,417-71,164,316 TMEM252-DT, LINC01506
    nsv6865431copy number variation1nstd229human GRCh38 chr9: 68,546,738-68,563,769 , GRCh37.p13 chr9: 71,161,654-71,178,685 TMEM252-DT, LINC01506
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6453231copy number variation1nstd223human GRCh38 chr9: 68,546,738-68,563,766 , GRCh37.p13 chr9: 71,161,654-71,178,682 TMEM252-DT, LINC01506
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6137093copy number variation1nstd213human GRCh37 chr9: 70,940,000-71,750,001 , GRCh38.p12 chr9: 68,325,084-69,135,085 FXN, PGM5, 16 more genes
    nsv5476949copy number variation1nstd206human GRCh37.p13 chr9|NW_003871067.1: 215,000-295,379 , GRCh38 chr9: 68,435,552-68,584,552 , GRCh37.p13 chr9: 71,050,468-71,130,847 LINC01506, TMEM252-DT, 2 more genes
    nsv4526449copy number variation1nstd166human GRCh37.p13 chr9: 71,108,999-71,379,000 , GRCh38.p12 chr9: 68,494,083-68,764,084 PGM5, PIP5K1B, 5 more genes
    nsv4481893mobile element insertion1nstd166human GRCh37.p13 chr9: 71,158,876-71,158,876 , GRCh38.p12 chr9: 68,543,960-68,543,960 TMEM252-DT, LINC01506
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4421062copy number variation1nstd174human GRCh37 chr9: 71,009,095-71,200,407 , GRCh38.p12 chr9: 68,394,179-68,585,491 LINC01506, PGM5, 3 more genes
    nsv4371052copy number variation3nstd173human GRCh37 chr9: 71,050,682-71,196,279 , GRCh38.p12 chr9: 68,435,766-68,581,363 LINC01506, TMEM252, 2 more genes
    nsv4178799copy number variation1nstd166human GRCh37.p13 chr9: 71,109,000-71,199,000 , GRCh38.p12 chr9: 68,494,084-68,584,084 TMEM252-DT, PGM5, 2 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