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 92

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5944179copy number variation1nstd209human GRCh38 chr16: 20,320,227-20,320,355 , GRCh37.p13 chr16: 20,331,549-20,331,677 GP2
    nsv5725173mobile element insertion1nstd211human GRCh38 chr16: 20,325,781-20,325,781 , GRCh37.p13 chr16: 20,337,103-20,337,103 GP2
    nsv5365542translocation1nstd200human GRCh38 chr16: 20,325,688-20,325,688 , GRCh38 chr16: 20,609,015-20,609,015 , GRCh37.p13 chr16: 20,620,337-20,620,337 , GRCh37.p13 chr16: 20,337,010-20,337,010 LOC107984831, GP2
    nsv5337868translocation1nstd200human GRCh37 chr16: 20,337,010-20,337,010 , GRCh37 chr16: 20,620,337-20,620,337 , GRCh38.p12 chr16: 20,325,688-20,325,688 , GRCh38.p12 chr16: 20,609,015-20,609,015 LOC107984831, GP2
    nsv5140662mobile element insertion1nstd203human GRCh38 chr16: 20,317,557-20,317,569 , GRCh37.p13 chr16: 20,328,879-20,328,891 GP2
    nsv5003094copy number variation1nstd200human GRCh38 chr16: 20,310,535-20,311,794 , GRCh37.p13 chr16: 20,321,857-20,323,116 GP2
    nsv4994528copy number variation1nstd200human GRCh38 chr16: 20,171,167-20,520,362 , GRCh37.p13 chr16: 20,182,489-20,531,684 LOC102723396, LOC105371119, 6 more genes
    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
    nsv4532397copy number variation1nstd166human GRCh37.p13 chr16: 20,336,999-20,423,000 , GRCh38.p12 chr16: 20,325,677-20,411,678 UMOD, ACSM5, 2 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
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4250158copy number variation1nstd166human GRCh37.p13 chr16: 20,146,232-20,522,596 , GRCh38.p12 chr16: 20,134,910-20,511,274 GP2, UMOD, 7 more genes
    nsv4244216copy number variation1nstd166human GRCh37.p13 chr16: 20,321,857-20,323,116 , GRCh38.p12 chr16: 20,310,535-20,311,794 GP2
    nsv4241181copy number variation1nstd166human GRCh37.p13 chr16: 20,337,000-20,344,000 , GRCh38.p12 chr16: 20,325,678-20,332,678 UMOD, GP2
    nsv3917467copy number variation1nstd102humanUncertain significance GRCh38 chr16: 20,229,045-20,627,132 , NCBI36 chr16: 20,147,868-20,545,955 , GRCh37 chr16: 20,240,367-20,638,454 LOC102723396, GP2, 12 more genes
    nsv3917409copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,956,252-28,225,665 , GRCh37 chr16: 15,048,751-28,318,164 , GRCh38 chr16: 14,954,894-28,306,843 SLC7A5P2, TRL-TAG3-1, 251 more genes
    nsv3913284copy number variation1nstd102humanUncertain significance GRCh38 chr16: 19,910,619-20,433,405 , GRCh37 chr16: 19,921,941-20,444,727 , NCBI36 chr16: 19,829,442-20,352,228 GP2, LOC102723396, 8 more genes
    nsv3910441copy number variation1nstd102humanPathogenic NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820 LOC729945, LOC102723728, 450 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