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 103

    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
    nsv7060237inversion1nstd229human GRCh38 chr16: 19,706,819-19,710,588 , GRCh37.p13 chr16: 19,718,141-19,721,910 KNOP1
    nsv6996614copy number variation1nstd229human GRCh38 chr16: 19,697,141-19,702,687 , GRCh37.p13 chr16: 19,708,463-19,714,009 VPS35L, KNOP1
    nsv6993076copy number variation1nstd229human GRCh38 chr16: 19,709,929-19,715,323 , GRCh37.p13 chr16: 19,721,251-19,726,645 IQCK, KNOP1
    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
    nsv6504782copy number variation1nstd223human GRCh38 chr16: 19,649,703-19,764,765 , GRCh37.p13 chr16: 19,661,025-19,776,087 KNOP1, VPS35L, 2 more genes
    nsv6496561copy number variation1nstd223human GRCh38 chr16: 19,709,901-19,715,800 , GRCh37.p13 chr16: 19,721,223-19,727,122 KNOP1, IQCK
    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
    nsv6133013copy number variation1nstd213human GRCh37 chr16: 19,620,000-22,460,001 , GRCh38.p12 chr16: 19,608,678-22,448,680 CDR2, CRYM, 76 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5940413copy number variation1nstd209human GRCh38 chr16: 19,707,806-19,707,912 , GRCh37.p13 chr16: 19,719,128-19,719,234 KNOP1
    nsv5003071copy number variation1nstd200human GRCh38 chr16: 19,709,927-19,715,307 , GRCh37.p13 chr16: 19,721,249-19,726,629 KNOP1, IQCK
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4426860copy number variation1nstd174human GRCh37 chr16: 19,718,563-19,719,446 , GRCh38.p12 chr16: 19,707,241-19,708,124 KNOP1
    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