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Items: 1 to 20 of 206

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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
    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
    nsv6134581copy number variation1nstd213human GRCh37 chr22: 17,410,000-17,630,001 , GRCh38.p12 chr22: 16,929,110-17,149,111 IGKV1OR22-1, IL17RA, 8 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
    nsv6112787copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,443,623-17,663,651 , GRCh38.p12 chr22: 16,962,733-17,182,761 IL17RA, HDHD5, 9 more genes
    nsv6056116copy number variation1nstd212human GRCh38 chr22: 17,038,072-17,040,380 , GRCh37.p13 chr22: 17,518,962-17,521,270 CECR7
    nsv6055369copy number variation1nstd212human GRCh38 chr22: 17,049,349-17,050,993 , GRCh37.p13 chr22: 17,530,239-17,531,883 CECR7
    nsv5592669copy number variation1nstd207human GRCh38 chr22: 17,038,567-17,039,026 , GRCh37.p13 chr22: 17,519,457-17,519,916 CECR7
    nsv5354432translocation1nstd200human GRCh38 chr10: 100,092,157-100,092,157 , GRCh38 chr22: 17,045,879-17,045,879 , GRCh37.p13 chr10: 101,851,914-101,851,914 , GRCh37.p13 chr22: 17,526,769-17,526,769 CECR7
    nsv5189629mobile element insertion1nstd203human GRCh38 chr22: 17,045,860-17,045,879 , GRCh37.p13 chr22: 17,526,750-17,526,769 CECR7
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