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 396

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7096084copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,119,651-62,159,505 , GRCh38.p12 chr20: 63,488,298-63,528,152 EEF1A2, LOC102723814, 3 more genes
    nsv7096082copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr20: 61,978,090-62,324,656 , GRCh38.p12 chr20: 63,346,738-63,693,303 SRMS, KCNQ2, 17 more genes
    nsv7095915copy number variation2nstd102humanPathogenic GRCh37 chr20: 62,075,992-62,324,656 , GRCh38.p12 chr20: 63,444,639-63,693,303 LOC105372725, PPDPF, 13 more genes
    nsv7065985inversion1nstd229human GRCh38 chr20: 63,509,212-64,282,670 , GRCh37.p13 chr20: 62,140,565-62,914,023 RNU1-134P, MIR6813, 46 more genes
    nsv7061289inversion1nstd229human GRCh38 chr20: 63,026,492-64,008,482 , GRCh37.p13 chr20: 61,657,844-62,639,835 TNFRSF6B, MIR941-5, 60 more genes
    nsv7059476inversion1nstd229human GRCh38 chr20: 63,024,183-64,005,567 , GRCh37.p13 chr20: 61,655,535-62,636,920 RTEL1-TNFRSF6B, LOC105372721, 60 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7034004copy number variation1nstd229human GRCh38 chr20: 63,535,040-63,542,376 , GRCh37.p13 chr20: 62,166,393-62,173,729 SRMS, PTK6
    nsv7029960copy number variation1nstd229human GRCh38 chr20: 63,534,701-63,539,800 , GRCh37.p13 chr20: 62,166,054-62,171,153 SRMS, PTK6
    nsv7028993copy number variation1nstd229human GRCh38 chr20: 63,442,601-63,572,200 , GRCh37.p13 chr20: 62,073,954-62,203,553 PTK6, HELZ2, 8 more genes
    nsv7026192copy number variation1nstd229human GRCh38 chr20: 63,529,683-63,533,397 , GRCh37.p13 chr20: 62,161,036-62,164,750 PTK6
    nsv7026176copy number variation1nstd229human GRCh38 chr20: 63,527,101-63,542,400 , GRCh37.p13 chr20: 62,158,454-62,173,753 SRMS, PTK6
    nsv7026165copy number variation1nstd229human GRCh38 chr20: 63,512,548-63,545,770 , GRCh37.p13 chr20: 62,143,901-62,177,123 LOC102723814, PTK6, 2 more genes
    nsv7024253copy number variation1nstd229human GRCh38 chr20: 63,356,301-63,572,200 , GRCh37.p13 chr20: 61,987,653-62,203,553 PTK6, EEF1A2, 12 more genes
    nsv7023436copy number variation1nstd229human GRCh38 chr20: 63,529,333-63,572,508 , GRCh37.p13 chr20: 62,160,686-62,203,861 PTK6, HELZ2, 2 more genes
    nsv7021271copy number variation1nstd229human GRCh38 chr20: 63,534,627-63,539,781 , GRCh37.p13 chr20: 62,165,980-62,171,134 PTK6, SRMS
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 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