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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993261copy number variation1nstd229human GRCh38 chr16: 83,808,389-83,827,138 , GRCh37.p13 chr16: 83,841,994-83,860,743 HSBP1
    nsv6989492copy number variation1nstd229human GRCh38 chr16: 83,819,822-83,827,060 , GRCh37.p13 chr16: 83,853,427-83,860,665 HSBP1
    nsv6989178copy number variation1nstd229human GRCh38 chr16: 83,789,538-83,851,097 , GRCh37.p13 chr16: 83,823,143-83,884,702 HSBP1, CDH13, 1 more genes
    nsv6985447copy number variation1nstd229human GRCh38 chr16: 83,476,239-83,857,093 , GRCh37.p13 chr16: 83,509,844-83,890,698 , CDH13-AS2, 3 more genes
    nsv6985076copy number variation1nstd229human GRCh38 chr16: 83,797,571-83,826,126 , GRCh37.p13 chr16: 83,831,176-83,859,731 CDH13, HSBP1, 1 more genes
    nsv6978539copy number variation1nstd229human GRCh38 chr16: 83,817,541-83,895,593 , GRCh37.p13 chr16: 83,851,146-83,929,198 HSBP1
    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
    nsv6623545copy number variation1nstd224human GRCh37 chr16: 83,762,106-83,876,991 , GRCh38.p12 chr16: 83,728,501-83,843,386 , CDH13, 2 more genes
    nsv6508483copy number variation1nstd223human GRCh38 chr16: 83,819,609-83,820,481 , GRCh37.p13 chr16: 83,853,214-83,854,086 HSBP1
    nsv6506920copy number variation1nstd223human GRCh38 chr16: 83,789,538-83,851,097 , GRCh37.p13 chr16: 83,823,143-83,884,702 CDH13, HSBP1, 1 more genes
    nsv6503433copy number variation1nstd223human GRCh38 chr16: 83,518,315-83,941,761 , GRCh37.p13 chr16: 83,551,920-83,975,366 , MLYCD, 4 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6314127copy number variation1nstd102humanUncertain significance GRCh37 chr16: 83,313,106-84,608,026 , GRCh38.p12 chr16: 83,279,501-84,574,420 TAF1C, LOC648774, 23 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6272381copy number variation1nstd214human GRCh38 chr16: 83,814,153-83,814,207 , GRCh37.p13 chr16: 83,847,758-83,847,812 HSBP1
    nsv6133210copy number variation1nstd213human GRCh37 chr16: 78,970,000-88,180,001 , GRCh38.p12 chr16: 78,936,103-88,146,395 , CA5A, 152 more genes
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