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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098931copy number variation1nstd102humanPathogenic GRCh38 chr22: 16,804,110-18,162,024 , GRCh37.p13 chr22: 17,285,000-18,644,791 SLC25A18, LINC01634, 44 more genes
    nsv7095928copy number variation2nstd102humanPathogenic GRCh37 chr22: 17,565,982-20,052,185 , GRCh38.p12 chr22: 17,085,092-20,064,662 CA15P1, BID, 103 more genes
    nsv7095815copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,565,982-18,613,903 , GRCh38.p12 chr22: 17,085,092-18,131,136 HDHD5, LINC01664, 30 more genes
    nsv6637923copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-18,916,828 , GRCh38.p12 chr22: 16,408,174-18,929,315 ANKRD62P1, IGKV1OR22-1, 87 more genes
    nsv6637806copy number variation1nstd102humanUncertain significance GRCh37 chr22: 16,888,900-17,597,713 , GRCh38.p12 chr22: 16,408,174-17,116,823 GPM6BP3, CHEK2P4, 29 more genes
    nsv6637694copy number variation1nstd102humanUncertain significance GRCh37 chr22: 16,888,900-17,948,922 , GRCh38.p12 chr22: 16,408,174-17,469,880 HDHD5, LINC01665, 41 more genes
    nsv6637447copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,570,796-19,695,101 , GRCh38.p12 chr22: 17,089,906-19,707,578 FAM230J, RN7SL168P, 88 more genes
    nsv6637415copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,034,543-17,948,922 , GRCh38.p12 chr22: 16,553,653-17,469,880 IGKV2OR22-4, RPL31P62, 37 more genes
    nsv6637374copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-18,649,190 , GRCh38.p12 chr22: 16,408,174-18,166,423 KCNMB3P1, CECR7, 59 more genes
    nsv6627030copy number variation1nstd224human GRCh37 chr22: 17,055,569-17,619,393 , GRCh38.p12 chr22: 16,574,679-17,138,503 IL17RA, XKR3, 27 more genes
    nsv6626897copy number variation1nstd224human GRCh37 chr22: 17,073,119-17,584,454 , GRCh38.p12 chr22: 16,592,229-17,103,564 IL17RA, XKR3, 22 more genes
    nsv6315558copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-21,915,509 , GRCh38.p12 chr22: 16,408,173-21,561,220 LINC01665, RN7SKP221, 209 more genes
    nsv6314752copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-18,644,241 , GRCh38.p12 chr22: 16,408,173-18,161,474 VN1R9P, LOC107985573, 59 more genes
    nsv6291520copy number variation1nstd102humanUncertain significance GRCh37 chr22: 16,888,900-17,619,816 , GRCh38.p12 chr22: 16,408,174-17,138,926 LOC100422375, IL17RA, 31 more genes
    nsv6290000copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,850,000-18,885,000 , GRCh38.p12 chr22: 16,369,338-18,897,487 VN1R9P, TUBA8, 86 more genes
    nsv6227168copy number variation1nstd214human GRCh38 chr22: 17,103,718-17,103,879 , GRCh37.p13 chr22: 17,584,608-17,584,769 IL17RA
    nsv6225963copy number variation1nstd214human GRCh38 chr22: 17,103,730-17,103,850 , GRCh37.p13 chr22: 17,584,620-17,584,740 IL17RA
    nsv6217893copy number variation1nstd214human GRCh38 chr22: 17,103,851-17,103,973 , GRCh37.p13 chr22: 17,584,741-17,584,863 IL17RA
    nsv6214652copy number variation1nstd214human GRCh38 chr22: 17,103,690-17,103,851 , GRCh37.p13 chr22: 17,584,580-17,584,741 IL17RA
    nsv6208201copy number variation1nstd214human GRCh38 chr22: 17,103,663-17,103,783 , GRCh37.p13 chr22: 17,584,553-17,584,673 IL17RA
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