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Items: 1 to 20 of 440

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131520insertion1nstd186human GRCh37 chr19: 34,737,059-34,737,059 , GRCh38.p12 chr19: 34,246,154-34,246,154 , GRCh38.p12 chr19|NW_003315963.1: 93,901-93,901 0
    nsv6130265insertion1nstd186human GRCh37 chr19: 34,704,087-34,704,123 , GRCh38.p12 chr19: 34,213,182-34,213,218 , GRCh38.p12 chr19|NW_003315963.1: 60,923-60,959 LSM14A
    nsv5384647mobile element deletion1nstd186human GRCh37 chr19: 34,774,753-34,775,039 , GRCh38.p12 chr19: 34,283,848-34,284,134 , GRCh38.p12 chr19|NW_003315963.1: 138,762-139,048 GARRE1
    nsv5345353translocation1nstd200human GRCh37 chr19: 34,663,668-34,663,668 , GRCh37 chr19: 34,685,380-34,685,380 , GRCh38.p12 chr19: 34,172,763-34,172,763 , GRCh38.p12 chr19|NW_003315963.1: 42,216-42,216 , GRCh38.p12 chr19: 34,194,475-34,194,475 , GRCh38.p12 chr19|NW_003315963.1: 20,504-20,504 LSM14A
    nsv5337711translocation1nstd200human GRCh37 chr19: 34,737,049-34,737,049 , GRCh37 chr19: 34,739,685-34,739,685 , GRCh38.p12 chr19|NW_003315963.1: 103,694-103,694 , GRCh38.p12 chr19|NW_003315963.1: 93,891-93,891 , GRCh38.p12 chr19: 34,246,144-34,246,144 , GRCh38.p12 chr19: 34,248,780-34,248,780 0
    nsv5329716translocation1nstd200human GRCh37 chr19: 34,730,612-34,730,612 , GRCh37 chr19: 34,727,601-34,727,601 , GRCh38.p12 chr19: 34,236,696-34,236,696 , GRCh38.p12 chr19|NW_003315963.1: 87,455-87,455 , GRCh38.p12 chr19: 34,239,707-34,239,707 , GRCh38.p12 chr19|NW_003315963.1: 84,444-84,444 0
    nsv4865126copy number variation1nstd200human GRCh37 chr19: 34,649,082-34,649,552 , GRCh38.p12 chr19|NW_003315963.1: 5,918-6,388 , GRCh38.p12 chr19: 34,158,177-34,158,647 0
    nsv4861304copy number variation1nstd200human GRCh37 chr19: 34,788,021-34,789,118 , GRCh38.p12 chr19: 34,297,116-34,298,213 , GRCh38.p12 chr19|NW_003315963.1: 152,030-153,127 GARRE1, RPL29P33
    nsv4861303copy number variation1nstd200human GRCh37 chr19: 34,670,505-34,675,063 , GRCh38.p12 chr19: 34,179,600-34,184,158 , GRCh38.p12 chr19|NW_003315963.1: 27,341-31,899 LSM14A
    nsv4861302copy number variation1nstd200human GRCh37 chr19: 34,665,145-34,666,361 , GRCh38.p12 chr19: 34,174,240-34,175,456 , GRCh38.p12 chr19|NW_003315963.1: 21,981-23,197 LSM14A
    nsv4861301copy number variation1nstd200human GRCh37 chr19: 34,648,059-34,649,862 , GRCh38.p12 chr19: 34,157,154-34,158,957 , GRCh38.p12 chr19|NW_003315963.1: 4,895-6,698 0
    nsv4769811mobile element deletion1nstd200human GRCh37 chr19: 34,774,751-34,775,042 , GRCh38.p12 chr19: 34,283,846-34,284,137 , GRCh38.p12 chr19|NW_003315963.1: 138,760-139,051 GARRE1
    nsv4769068insertion1nstd186human GRCh37 chr19: 34,737,049-34,737,049 , GRCh38.p12 chr19: 34,246,144-34,246,144 , GRCh38.p12 chr19|NW_003315963.1: 93,891-93,891 0
    nsv4754780insertion1nstd199human GRCh37 chr19: 34,737,049-34,737,049 , GRCh38.p12 chr19: 34,246,144-34,246,144 , GRCh38.p12 chr19|NW_003315963.1: 93,891-93,891 0
    nsv4747977copy number variation1nstd199human GRCh37 chr19: 34,743,267-34,743,568 , GRCh38.p12 chr19: 34,252,362-34,252,663 , GRCh38.p12 chr19|NW_003315963.1: 107,276-107,577 GARRE1
    nsv4721237insertion1nstd186human GRCh37 chr19: 34,704,073-34,704,073 , GRCh38.p12 chr19: 34,213,168-34,213,168 , GRCh38.p12 chr19|NW_003315963.1: 60,909-60,909 LSM14A
    nsv4691632mobile element insertion1nstd186human GRCh37 chr19: 34,704,087-34,704,087 , GRCh38.p12 chr19|NW_003315963.1: 60,923-60,923 , GRCh38.p12 chr19: 34,213,182-34,213,182 LSM14A
    nsv4685315insertion1nstd194human GRCh37 chr19: 34,737,049-34,737,049 , GRCh38.p12 chr19: 34,246,144-34,246,144 , GRCh38.p12 chr19|NW_003315963.1: 93,891-93,891 0
    nsv4670697copy number variation1nstd186human GRCh37 chr19: 34,728,611-34,730,126 , GRCh38.p12 chr19: 34,237,706-34,239,221 , GRCh38.p12 chr19|NW_003315963.1: 85,454-86,969 0
    nsv4668590copy number variation1nstd186human GRCh37 chr19: 34,727,601-34,730,612 , GRCh38.p12 chr19: 34,236,696-34,239,707 , GRCh38.p12 chr19|NW_003315963.1: 84,444-87,455 0
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