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Items: 1 to 20 of 587

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    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
    nsv7146740insertion1nstd232human GRCh37.p13 chr20: 62,197,972-62,197,972 , GRCh38.p12 chr20: 63,566,619-63,566,619 HELZ2
    nsv7141808copy number variation1nstd232human GRCh37.p13 chr20: 62,192,050-62,192,146 , GRCh38.p12 chr20: 63,560,697-63,560,793 HELZ2
    nsv7137881insertion1nstd232human GRCh37.p13 chr20: 62,197,918-62,197,918 , GRCh38.p12 chr20: 63,566,565-63,566,565 HELZ2
    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
    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
    nsv7033380copy number variation1nstd229human GRCh38 chr20: 63,574,621-63,577,639 , GRCh37.p13 chr20: 62,205,974-62,208,992 HELZ2
    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
    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
    nsv7021975copy number variation1nstd229human GRCh38 chr20: 63,565,601-63,567,700 , GRCh37.p13 chr20: 62,196,954-62,199,053 HELZ2
    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
    nsv6635293copy number variation1nstd227human GRCh37 chr20: 62,109,405-62,201,784 , GRCh38.p12 chr20: 63,478,052-63,570,431 EEF1A2, PTK6, 6 more genes
    nsv6635284copy number variation1nstd227human GRCh37 chr20: 62,119,121-62,201,784 , GRCh38.p12 chr20: 63,487,768-63,570,431 EEF1A2, PTK6, 6 more genes
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