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Items: 1 to 20 of 786

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970204insertion1nstd209human GRCh38 chr22: 43,675,317-43,675,317 , GRCh37.p13 chr22: 44,071,197-44,071,197 EFCAB6
    nsv5963933copy number variation1nstd209human GRCh38 chr22: 43,630,854-43,631,964 , GRCh37.p13 chr22: 44,026,734-44,027,844 EFCAB6
    nsv5963728copy number variation1nstd209human GRCh38 chr22: 43,718,551-43,947,128 , GRCh37.p13 chr22: 44,114,431-44,343,008 , HMGN2P9, 7 more genes
    nsv5962643copy number variation1nstd209human GRCh38 chr22: 43,635,554-43,643,984 , GRCh37.p13 chr22: 44,031,434-44,039,864 YWHAQP2, EFCAB6
    nsv5961133copy number variation1nstd209human GRCh38 chr22: 43,545,809-43,551,846 , GRCh37.p13 chr22: 43,941,689-43,947,726 EFCAB6
    nsv5959399copy number variation1nstd209human GRCh38 chr22: 43,686,868-43,686,947 , GRCh37.p13 chr22: 44,082,748-44,082,827 EFCAB6
    nsv5957496copy number variation1nstd209human GRCh38 chr22: 43,656,713-43,656,811 , GRCh37.p13 chr22: 44,052,593-44,052,691 EFCAB6
    nsv5956868copy number variation1nstd209human GRCh38 chr22: 43,589,159-43,589,529 , GRCh37.p13 chr22: 43,985,039-43,985,409 EFCAB6
    nsv5953136copy number variation1nstd209human GRCh38 chr22: 43,526,809-43,526,860 , GRCh37.p13 chr22: 43,922,689-43,922,740 EFCAB6, EFCAB6-AS1
    nsv5951029copy number variation1nstd209human GRCh38 chr22: 43,738,276-43,738,327 , GRCh37.p13 chr22: 44,134,156-44,134,207 EFCAB6
    nsv5948025copy number variation1nstd209human GRCh38 chr22: 43,578,965-43,579,644 , GRCh37.p13 chr22: 43,974,845-43,975,524 EFCAB6
    nsv5947906copy number variation1nstd209human GRCh38 chr22: 43,634,092-43,636,574 , GRCh37.p13 chr22: 44,029,972-44,032,454 EFCAB6
    nsv5886775copy number variation2nstd209human GRCh38 chr22: 43,675,874-43,678,585 , GRCh37.p13 chr22: 44,071,754-44,074,465 EFCAB6
    nsv5885334copy number variation1nstd209human GRCh38 chr22: 43,705,994-43,718,636 , GRCh37.p13 chr22: 44,101,874-44,114,516 EFCAB6
    nsv5883483copy number variation2nstd209human GRCh38 chr22: 43,630,784-43,631,983 , GRCh37.p13 chr22: 44,026,664-44,027,863 EFCAB6
    nsv5881066copy number variation2nstd209human GRCh38 chr22: 43,634,034-43,636,890 , GRCh37.p13 chr22: 44,029,914-44,032,770 EFCAB6
    nsv5878773copy number variation2nstd209human GRCh38 chr22: 43,545,666-43,551,865 , GRCh37.p13 chr22: 43,941,546-43,947,745 EFCAB6
    nsv5877144copy number variation1nstd209human GRCh38 chr22: 43,630,176-43,682,285 , GRCh37.p13 chr22: 44,026,056-44,078,165 EFCAB6, YWHAQP2
    nsv5875065copy number variation1nstd209human GRCh38 chr22: 43,584,316-43,586,441 , GRCh37.p13 chr22: 43,980,196-43,982,321 EFCAB6
    nsv5870100copy number variation2nstd209human GRCh38 chr22: 43,634,684-43,637,540 , GRCh37.p13 chr22: 44,030,564-44,033,420 EFCAB6
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