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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
    nsv6627033copy number variation1nstd224human GRCh37 chr22: 17,061,371-17,289,118 , GRCh38.p12 chr22: 16,580,481-16,808,228 VWFP1, KCNMB3P1, 9 more genes
    nsv6627032copy number variation1nstd224human GRCh37 chr22: 17,058,616-17,289,118 , GRCh38.p12 chr22: 16,577,726-16,808,228 VWFP1, LINC01665, 9 more genes
    nsv6627031copy number variation3nstd224human GRCh37 chr22: 17,056,038-17,289,118 , GRCh38.p12 chr22: 16,575,148-16,808,228 VWFP1, XKR3, 9 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
    nsv6627028copy number variation23nstd224human GRCh37 chr22: 16,855,618-17,289,118 , GRCh38.p12 chr22: 16,374,956-16,808,228 XKR3, TPTEP1, 15 more genes
    nsv6626898copy number variation1nstd224human GRCh37 chr22: 17,073,185-17,289,118 , GRCh38.p12 chr22: 16,592,295-16,808,228 VWFP1, LINC01665, 8 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
    nsv6626896copy number variation1nstd224human GRCh37 chr22: 17,061,371-17,271,797 , GRCh38.p12 chr22: 16,580,481-16,790,907 XKR3, TPTEP1, 9 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
    nsv6626893copy number variation2nstd224human GRCh37 chr22: 17,055,569-17,289,118 , GRCh38.p12 chr22: 16,574,679-16,808,228 TPTEP1, VWFP1, 10 more genes
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