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 387

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6858010copy number variation1nstd229human GRCh38 chr8: 37,411,512-37,415,003 , GRCh37.p13 chr8: 37,269,030-37,272,521 LINC01605
    nsv6854343copy number variation1nstd229human GRCh38 chr8: 37,504,827-37,509,767 , GRCh37.p13 chr8: 37,362,345-37,367,285 LINC01605
    nsv6853779copy number variation1nstd229human GRCh38 chr8: 37,493,429-37,502,126 , GRCh37.p13 chr8: 37,350,947-37,359,644 LINC01605
    nsv6851058copy number variation1nstd229human GRCh38 chr8: 37,509,847-37,513,696 , GRCh37.p13 chr8: 37,367,365-37,371,214 LINC01605
    nsv6850836copy number variation1nstd229human GRCh38 chr8: 37,467,082-37,477,560 , GRCh37.p13 chr8: 37,324,600-37,335,078 LINC01605
    nsv6850748copy number variation1nstd229human GRCh38 chr8: 37,442,307-37,657,111 , GRCh37.p13 chr8: 37,299,825-37,514,629 LOC105379378, LOC105379380, 2 more genes
    nsv6850542copy number variation1nstd229human GRCh38 chr8: 37,481,074-37,483,013 , GRCh37.p13 chr8: 37,338,592-37,340,531 LINC01605
    nsv6848830copy number variation1nstd229human GRCh38 chr8: 37,448,553-37,454,707 , GRCh37.p13 chr8: 37,306,071-37,312,225 LINC01605
    nsv6845653copy number variation1nstd229human GRCh38 chr8: 37,447,778-37,452,584 , GRCh37.p13 chr8: 37,305,296-37,310,102 LINC01605
    nsv6845029copy number variation1nstd229human GRCh38 chr8: 37,420,389-37,431,311 , GRCh37.p13 chr8: 37,277,907-37,288,829 LINC01605
    nsv6843893copy number variation1nstd229human GRCh38 chr8: 37,451,904-37,452,148 , GRCh37.p13 chr8: 37,309,422-37,309,666 LINC01605
    nsv6842468copy number variation1nstd229human GRCh38 chr8: 37,428,315-37,434,641 , GRCh37.p13 chr8: 37,285,833-37,292,159 LINC01605
    nsv6842417copy number variation1nstd229human GRCh38 chr8: 37,482,502-37,486,979 , GRCh37.p13 chr8: 37,340,020-37,344,497 LINC01605
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6571507inversion1nstd223human GRCh38 chr8: 37,514,036-37,518,167 , GRCh37.p13 chr8: 37,371,554-37,375,685 LINC01605
    nsv6435237copy number variation1nstd223human GRCh38 chr8: 37,504,821-37,509,767 , GRCh37.p13 chr8: 37,362,339-37,367,285 LINC01605
    nsv6434837copy number variation1nstd223human GRCh38 chr8: 37,509,844-37,513,696 , GRCh37.p13 chr8: 37,367,362-37,371,214 LINC01605
    nsv6431528copy number variation1nstd223human GRCh38 chr8: 37,420,301-37,420,700 , GRCh37.p13 chr8: 37,277,819-37,278,218 LINC01605
    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