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Items: 1 to 20 of 186

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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
    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
    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
    nsv6627169copy number variation1nstd224human GRCh37 chr22: 17,301,217-17,329,601 , GRCh38.p12 chr22: 16,820,327-16,848,711 HSFY1P1, GPM6BP3, 1 more genes
    nsv6627168copy number variation1nstd224human GRCh37 chr22: 16,855,618-17,456,773 , GRCh38.p12 chr22: 16,374,956-16,975,883 IGKV3OR22-2, IGKV1OR22-1, 24 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
    nsv6627029copy number variation1nstd224human GRCh37 chr22: 16,897,695-17,319,156 , GRCh38.p12 chr22: 16,416,969-16,838,266 XKR3, TPTEP1, 16 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
    nsv6626895copy number variation1nstd224human GRCh37 chr22: 17,057,138-17,456,773 , GRCh38.p12 chr22: 16,576,248-16,975,883 XKR3, TPTEP1, 18 more genes
    nsv6626894copy number variation1nstd224human GRCh37 chr22: 17,056,038-17,327,157 , GRCh38.p12 chr22: 16,575,148-16,846,267 XKR3, TPTEP1, 11 more genes
    nsv6626891copy number variation1nstd224human GRCh37 chr22: 16,855,618-17,399,211 , GRCh38.p12 chr22: 16,374,956-16,918,321 ABCD1P4, SLC9B1P4, 20 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
    nsv6291733copy number variation1nstd102humanLikely benign GRCh37 chr22: 16,964,385-17,358,927 , GRCh38.p12 chr22: 16,483,635-16,878,037 CCT8L2, FABP5P11, 16 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
    nsv6134205copy number variation1nstd213human GRCh37 chr22: 17,290,000-17,690,001 , GRCh38.p12 chr22: 16,809,110-17,209,111 IGKV1OR22-1, RPL32P5, 20 more genes
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