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 338

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7098189copy number variation1nstd102humanUncertain significance GRCh37 chr8: 97,156,791-97,345,794 , GRCh38.p12 chr8: 96,144,563-96,333,566 UQCRB-AS1, MTERF3, 4 more genes
    nsv7097674copy number variation1nstd102humanUncertain significance GRCh37 chr8: 96,037,237-97,345,794 , GRCh38.p12 chr8: 95,025,009-96,333,566 NDUFAF6, LINC01298, 19 more genes
    nsv7072181inversion1nstd229human GRCh38 chr8: 94,465,642-98,351,757 , GRCh37.p13 chr8: 95,477,870-99,363,985 SDC2, LOC100286997, 59 more genes
    nsv6857478copy number variation1nstd229human GRCh38 chr8: 96,336,019-96,339,563 , GRCh37.p13 chr8: 97,348,247-97,351,791 PTDSS1
    nsv6848483copy number variation1nstd229human GRCh38 chr8: 96,318,528-96,318,588 , GRCh37.p13 chr8: 97,330,756-97,330,816 PTDSS1
    nsv6846694copy number variation1nstd229human GRCh38 chr8: 96,332,434-96,341,615 , GRCh37.p13 chr8: 97,344,662-97,353,843 PTDSS1
    nsv6845859copy number variation1nstd229human GRCh38 chr8: 96,310,021-96,310,410 , GRCh37.p13 chr8: 97,322,249-97,322,638 PTDSS1
    nsv6843065copy number variation1nstd229human GRCh38 chr8: 96,336,601-96,339,600 , GRCh37.p13 chr8: 97,348,829-97,351,828 PTDSS1
    nsv6842445copy number variation1nstd229human GRCh38 chr8: 96,304,893-96,310,670 , GRCh37.p13 chr8: 97,317,121-97,322,898 PTDSS1
    nsv6839494copy number variation1nstd229human GRCh38 chr8: 96,334,667-96,356,738 , GRCh37.p13 chr8: 97,346,895-97,368,966 PTDSS1
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6633288copy number variation1nstd224human GRCh37 chr8: 97,269,192-97,285,617 , GRCh38.p12 chr8: 96,256,964-96,273,389 MTERF3, LOC105375652, 1 more genes
    nsv6433237copy number variation1nstd223human GRCh38 chr8: 96,310,254-96,310,927 , GRCh37.p13 chr8: 97,322,482-97,323,155 PTDSS1
    nsv6431999copy number variation1nstd223human GRCh38 chr8: 96,327,369-96,329,161 , GRCh37.p13 chr8: 97,339,597-97,341,389 PTDSS1
    nsv6430617copy number variation1nstd223human GRCh38 chr8: 96,316,744-96,318,074 , GRCh37.p13 chr8: 97,328,972-97,330,302 PTDSS1
    nsv6429227copy number variation1nstd223human GRCh38 chr8: 96,336,001-96,338,200 , GRCh37.p13 chr8: 97,348,229-97,350,428 PTDSS1
    nsv6429223copy number variation1nstd223human GRCh38 chr8: 96,310,004-96,310,505 , GRCh37.p13 chr8: 97,322,232-97,322,733 PTDSS1
    nsv6422593copy number variation1nstd223human GRCh38 chr8: 96,185,559-96,289,990 , GRCh37.p13 chr8: 97,197,787-97,302,218 MTERF3, LOC105375652, 3 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