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 166

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148086copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,895,517-135,440,296 , GRCh38.p12 chr10: 123,136,001-133,626,792 FANK1, LOC105378534, 159 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv7069141inversion1nstd229human GRCh38 chr10: 133,549,124-133,639,965 , GRCh37.p13 chr10: 135,362,628-135,453,469 SYCE1, OR6L1P, 4 more genes
    nsv6635856copy number variation1nstd227human GRCh38.p12 chr10: 133,438,843-133,740,558 , GRCh37 chr10: 135,252,347-135,477,883 CYP2E1, OR7M1P, 17 more genes
    nsv6635457copy number variation2nstd227human GRCh38.p12 chr10: 133,421,076-133,740,558 , GRCh37 chr10: 135,234,580-135,477,883 CYP2E1, OR7M1P, 20 more genes
    nsv6620273copy number variation1nstd224human GRCh37 chr10: 135,428,246-135,439,095 , GRCh38.p12 chr10: 133,614,742-133,625,591 FRG2B
    nsv6620271copy number variation3nstd224human GRCh37 chr10: 135,402,200-135,439,095 , GRCh38.p12 chr10: 133,588,696-133,625,591 FRG2B
    nsv6453780copy number variation1nstd223human GRCh38 chr10: 133,612,601-133,634,500 , GRCh37.p13 chr10: 135,426,105-135,448,004 FRG2B
    nsv6450661copy number variation1nstd223human GRCh38 chr10: 133,288,253-133,664,429 , GRCh37.p13 chr10: 135,101,757-135,477,791 MTG1, FRG2B, 22 more genes
    nsv6448632copy number variation1nstd223human GRCh38 chr10: 133,609,001-133,634,600 , GRCh37.p13 chr10: 135,422,505-135,448,104 FRG2B
    nsv6445212copy number variation1nstd223human GRCh38 chr10: 133,624,101-133,627,300 , GRCh37.p13 chr10: 135,437,605-135,440,804 FRG2B
    nsv6309141copy number variation1nstd102humanPathogenic GRCh37 chr10: 134,916,201-135,439,108 , GRCh38.p12 chr10: 133,102,697-133,625,604 FUOM, SCART1, 28 more genes
    nsv6131864copy number variation1nstd213human GRCh37 chr10: 135,070,000-135,534,747 , GRCh38.p12 chr10: 133,256,496-133,787,422 PAOX, DUX4L15, 37 more genes
    nsv6131861copy number variation1nstd213human GRCh37 chr10: 128,770,000-135,534,747 , GRCh38.p12 chr10: 126,971,736-133,787,422 ADAM8, BNIP3, 113 more genes
    nsv6131777copy number variation1nstd213human GRCh37 chr10: 133,750,000-135,534,747 , GRCh38.p12 chr10: 131,936,496-133,787,422 ADAM8, BNIP3, 69 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5854403copy number variation2nstd209human GRCh38 chr10: 133,612,882-133,622,681 , GRCh37.p13 chr10: 135,426,386-135,436,185 FRG2B
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5497134copy number variation1nstd206human GRCh38 chr10: 133,537,130-133,662,130 , GRCh37.p13 chr10: 135,350,634-135,475,634 CYP2E1, SYCE1, 6 more genes
    nsv5255604copy number variation1nstd204human GRCh38.p13 chr10: 133,611,182-133,632,761 , GRCh37.p13 chr10: 135,424,686-135,446,265 FRG2B
    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