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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094603copy number variation1nstd102humanUncertain significance GRCh37 chr16: 83,932,750-84,211,465 , GRCh38.p12 chr16: 83,899,145-84,177,859 NECAB2, HSDL1, 9 more genes
    nsv7076578inversion1nstd229human GRCh38 chr16: 83,742,713-84,033,267 , GRCh37.p13 chr16: 83,776,318-84,066,872 HSBP1, NECAB2, 6 more genes
    nsv7076150inversion1nstd229human GRCh38 chr16: 83,426,720-84,571,834 , GRCh37.p13 chr16: 83,460,325-84,605,440 , LOC648774, 23 more genes
    nsv7073806inversion1nstd229human GRCh38 chr16: 83,959,188-84,022,126 , GRCh37.p13 chr16: 83,992,793-84,055,731 SLC38A8, OSGIN1, 1 more genes
    nsv7069513inversion1nstd229human GRCh38 chr16: 83,832,179-84,528,985 , GRCh37.p13 chr16: 83,865,784-84,562,591 HSDL1, ATP2C2-AS1, 17 more genes
    nsv6995142copy number variation1nstd229human GRCh38 chr16: 83,870,301-84,028,700 , GRCh37.p13 chr16: 83,903,906-84,062,305 SLC38A8, MLYCD, 3 more genes
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993903copy number variation1nstd229human GRCh38 chr16: 83,896,130-84,027,702 , GRCh37.p13 chr16: 83,929,735-84,061,307 MLYCD, NECAB2, 3 more genes
    nsv6992668copy number variation1nstd229human GRCh38 chr16: 83,866,843-84,024,110 , GRCh37.p13 chr16: 83,900,448-84,057,715 SLC38A8, MLYCD, 3 more genes
    nsv6992485copy number variation1nstd229human GRCh38 chr16: 83,920,050-84,036,257 , GRCh37.p13 chr16: 83,953,655-84,069,862 SLC38A8, MLYCD, 3 more genes
    nsv6992361copy number variation1nstd229human GRCh38 chr16: 83,854,864-84,034,304 , GRCh37.p13 chr16: 83,888,469-84,067,909 LOC105371372, OSGIN1, 3 more genes
    nsv6989652copy number variation1nstd229human GRCh38 chr16: 83,870,081-84,053,349 , GRCh37.p13 chr16: 83,903,686-84,086,954 OSGIN1, NECAB2, 5 more genes
    nsv6988623copy number variation1nstd229human GRCh38 chr16: 83,936,713-84,051,371 , GRCh37.p13 chr16: 83,970,318-84,084,976 OSGIN1, SLC38A8, 2 more genes
    nsv6988057copy number variation1nstd229human GRCh38 chr16: 83,870,101-84,051,100 , GRCh37.p13 chr16: 83,903,706-84,084,705 MLYCD, SLC38A8, 4 more genes
    nsv6985269copy number variation1nstd229human GRCh38 chr16: 83,964,558-84,002,270 , GRCh37.p13 chr16: 83,998,163-84,035,875 OSGIN1, NECAB2
    nsv6982746copy number variation1nstd229human GRCh38 chr16: 83,894,667-83,979,433 , GRCh37.p13 chr16: 83,928,272-84,013,038 NECAB2, MLYCD, 2 more genes
    nsv6981903copy number variation1nstd229human GRCh38 chr16: 83,878,443-84,573,896 , GRCh37.p13 chr16: 83,912,048-84,607,502 KCNG4, ATP2C2-AS1, 18 more genes
    nsv6637658copy number variation1nstd102humanUncertain significance GRCh37 chr16: 82,943,629-84,073,053 , GRCh38.p12 chr16: 82,910,024-84,039,448 NECAB2, HSBP1, 10 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6591086inversion1nstd223human GRCh38 chr16: 83,950,712-83,951,781 , GRCh37.p13 chr16: 83,984,317-83,985,386 OSGIN1
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