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 145

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7068229inversion1nstd229human GRCh38 chr16: 19,547,685-19,547,697 , GRCh37.p13 chr16: 19,559,007-19,559,019 CCP110
    nsv6991322copy number variation1nstd229human GRCh38 chr16: 19,519,164-19,548,371 , GRCh37.p13 chr16: 19,530,486-19,559,693 CCP110, GDE1
    nsv6984019copy number variation1nstd229human GRCh38 chr16: 19,466,420-19,547,143 , GRCh37.p13 chr16: 19,477,742-19,558,465 CCP110, RNU4-46P, 2 more genes
    nsv6982030copy number variation1nstd229human GRCh38 chr16: 19,032,850-19,819,158 , GRCh37.p13 chr16: 19,044,172-19,830,480 COQ7, TMC5, 15 more genes
    nsv6978692copy number variation1nstd229human GRCh38 chr16: 19,494,962-19,759,954 , GRCh37.p13 chr16: 19,506,284-19,771,276 IQCK, KNOP1, 6 more genes
    nsv6966433copy number variation1nstd229human GRCh38 chr16: 17,335,724-19,726,946 , GRCh37.p13 chr16: 17,429,581-19,738,268 MIR3179-4, GDE1, 45 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6582241inversion1nstd223human GRCh38 chr16: 19,538,553-19,538,949 , GRCh37.p13 chr16: 19,549,875-19,550,271 CCP110
    nsv6576457inversion1nstd223human GRCh38 chr16: 19,538,584-19,539,071 , GRCh37.p13 chr16: 19,549,906-19,550,393 CCP110
    nsv6503089copy number variation1nstd223human GRCh38 chr16: 19,553,757-19,553,965 , GRCh37.p13 chr16: 19,565,079-19,565,287 CCP110, VPS35L
    nsv6500939copy number variation1nstd223human GRCh38 chr16: 19,466,420-19,547,137 , GRCh37.p13 chr16: 19,477,742-19,558,459 TMC5, GDE1, 2 more genes
    nsv6498872copy number variation1nstd223human GRCh38 chr16: 19,530,539-19,531,859 , GRCh37.p13 chr16: 19,541,861-19,543,181 CCP110
    nsv6133261copy number variation1nstd213human GRCh37 chr16: 19,140,000-21,360,001 , GRCh38.p12 chr16: 19,128,678-21,348,680 CRYM, GP2, 49 more genes
    nsv6133258copy number variation1nstd213human GRCh37 chr16: 16,530,000-21,500,001 , GRCh38.p12 chr16: 16,436,143-21,488,680 CRYM, GP2, 93 more genes
    nsv6133012copy number variation1nstd213human GRCh37 chr16: 19,370,000-19,700,001 , GRCh38.p12 chr16: 19,358,678-19,688,679 CCP110, GDE1, 4 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5306689copy number variation1nstd204human GRCh37.p13 chr16: 19,562,226-19,566,850 , GRCh38.p13 chr16: 19,550,904-19,555,528 VPS35L, CCP110
    nsv5272207copy number variation1nstd204human GRCh38.p13 chr16: 19,550,848-19,555,786 , GRCh37.p13 chr16: 19,562,170-19,567,108 CCP110, VPS35L
    nsv5265458copy number variation1nstd204human GRCh38.p13 chr16: 19,549,701-19,556,700 , GRCh37.p13 chr16: 19,561,023-19,568,022 VPS35L, CCP110
    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