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 353

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143575insertion1nstd232human GRCh37.p13 chr10: 74,831,938-74,831,938 , GRCh38.p12 chr10: 73,072,180-73,072,180 P4HA1
    nsv7140696insertion1nstd232human GRCh37.p13 chr10: 74,790,131-74,790,131 , GRCh38.p12 chr10: 73,030,373-73,030,373 P4HA1
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7058716inversion1nstd229human GRCh38 chr10: 72,663,272-73,189,528 , GRCh37.p13 chr10: 74,423,030-74,949,286 NUDT13, PLA2G12B, 10 more genes
    nsv6895194copy number variation1nstd229human GRCh38 chr10: 73,017,057-73,044,129 , GRCh37.p13 chr10: 74,776,815-74,803,887 P4HA1
    nsv6895110copy number variation1nstd229human GRCh38 chr10: 73,069,601-73,147,700 , GRCh37.p13 chr10: 74,829,359-74,907,458 P4HA1, ECD, 2 more genes
    nsv6893628copy number variation1nstd229human GRCh38 chr10: 72,714,112-73,254,102 , GRCh37.p13 chr10: 74,473,870-75,013,860 EIF4A2P2, MRPS16, 15 more genes
    nsv6892600copy number variation1nstd229human GRCh38 chr10: 73,082,850-73,083,074 , GRCh37.p13 chr10: 74,842,608-74,842,832 P4HA1
    nsv6891311copy number variation1nstd229human GRCh38 chr10: 73,030,111-73,032,113 , GRCh37.p13 chr10: 74,789,869-74,791,871 P4HA1
    nsv6889491copy number variation1nstd229human GRCh38 chr10: 73,062,769-73,066,310 , GRCh37.p13 chr10: 74,822,527-74,826,068 P4HA1
    nsv6887575copy number variation1nstd229human GRCh38 chr10: 73,038,627-73,038,925 , GRCh37.p13 chr10: 74,798,385-74,798,683 P4HA1
    nsv6886224copy number variation1nstd229human GRCh38 chr10: 72,960,619-73,068,204 , GRCh37.p13 chr10: 74,720,377-74,827,962 P4HA1, RPL17P50
    nsv6885823copy number variation1nstd229human GRCh38 chr10: 73,079,506-73,081,763 , GRCh37.p13 chr10: 74,839,264-74,841,521 P4HA1
    nsv6885174copy number variation1nstd229human GRCh38 chr10: 73,045,349-73,075,274 , GRCh37.p13 chr10: 74,805,107-74,835,032 P4HA1
    nsv6881917copy number variation1nstd229human GRCh38 chr10: 73,084,901-73,215,400 , GRCh37.p13 chr10: 74,844,659-74,975,158 EIF4A2P2, LOC105378358, 5 more genes
    nsv6595086inversion1nstd223human GRCh38 chr10: 73,048,439-73,048,838 , GRCh37.p13 chr10: 74,808,197-74,808,596 P4HA1
    nsv6594213inversion1nstd223human GRCh38 chr10: 73,048,027-73,048,322 , GRCh37.p13 chr10: 74,807,785-74,808,080 P4HA1
    nsv6592448inversion1nstd223human GRCh38 chr10: 73,040,616-73,041,371 , GRCh37.p13 chr10: 74,800,374-74,801,129 P4HA1
    nsv6589824inversion1nstd223human GRCh38 chr10: 73,086,848-73,087,271 , GRCh37.p13 chr10: 74,846,606-74,847,029 P4HA1
    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