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 400

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148108copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,256-15,492,591 , GRCh38.p12 chr17: 14,191,939-15,589,277 LOC105371545, TVP23C, 25 more genes
    nsv7148090copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,256-15,477,547 , GRCh38.p12 chr17: 14,191,939-15,574,233 TEKT3, CDRT15, 25 more genes
    nsv7098896copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,306-15,472,344 , GRCh38.p12 chr17: 14,191,989-15,569,030 CDRT4, LOC105371547, 25 more genes
    nsv7098894copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,306-15,466,762 , GRCh38.p12 chr17: 14,191,989-15,563,448 CDRT8, TVP23C, 24 more genes
    nsv7093401copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,110,127-15,472,344 , GRCh38.p12 chr17: 14,206,810-15,569,030 HS3ST3B1, PMP22, 25 more genes
    nsv7066148inversion1nstd229human GRCh38 chr17: 14,204,036-14,435,006 , GRCh37.p13 chr17: 14,107,353-14,338,323 LOC107985080, HS3ST3B1, 3 more genes
    nsv6992363copy number variation1nstd229human GRCh38 chr17: 14,337,998-14,338,509 , GRCh37.p13 chr17: 14,241,315-14,241,826 HS3ST3B1
    nsv6989082copy number variation1nstd229human GRCh38 chr17: 14,321,655-14,326,615 , GRCh37.p13 chr17: 14,224,972-14,229,932 HS3ST3B1
    nsv6983718copy number variation1nstd229human GRCh38 chr17: 14,320,070-14,328,532 , GRCh37.p13 chr17: 14,223,387-14,231,849 HS3ST3B1
    nsv6979493copy number variation1nstd229human GRCh38 chr17: 14,339,341-14,339,714 , GRCh37.p13 chr17: 14,242,658-14,243,031 HS3ST3B1
    nsv6979351copy number variation1nstd229human GRCh38 chr17: 12,688,917-15,327,390 , GRCh37.p13 chr17: 12,592,234-15,230,707 PMP22, COX10-DT, 32 more genes
    nsv6638035copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,934-15,484,630 , GRCh38.p12 chr17: 14,184,617-15,581,316 COX10, CDRT15, 25 more genes
    nsv6637965copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,083,055-15,484,859 , GRCh38.p12 chr17: 14,179,738-15,581,545 CDRT8, LOC105371545, 25 more genes
    nsv6637912copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,073,563-15,479,923 , GRCh38.p12 chr17: 14,170,246-15,576,609 TVP23C-CDRT4, LOC101928475, 25 more genes
    nsv6637838copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,082,945-15,484,858 , GRCh38.p12 chr17: 14,179,628-15,581,544 COX10, FBXW10B, 25 more genes
    nsv6637794copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,078,283-15,479,940 , GRCh38.p12 chr17: 14,174,966-15,576,626 LOC105371545, TVP23C, 25 more genes
    nsv6637650copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,083,055-15,483,608 , GRCh38.p12 chr17: 14,179,738-15,580,294 MGC12916, RPL9P2, 25 more genes
    nsv6637617copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,934-15,491,532 , GRCh38.p12 chr17: 14,184,617-15,588,218 MGC12916, RPL9P2, 25 more genes
    nsv6637613copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,788-15,484,858 , GRCh38.p12 chr17: 14,184,471-15,581,544 TVP23C-CDRT4, LOC105371547, 25 more genes
    nsv6637590copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,934-15,479,940 , GRCh38.p12 chr17: 14,184,617-15,576,626 LOC105371545, RN7SL792P, 25 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