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Items: 1 to 20 of 1219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131584insertion1nstd186human GRCh37 chr19: 20,984,702-20,984,702 , GRCh38.p12 chr19|NW_003315962.1: 138,483-138,483 , GRCh38.p12 chr19: 20,801,896-20,801,896 ZNF66
    nsv6131019insertion1nstd186human GRCh37 chr19: 21,063,131-21,063,131 , GRCh38.p12 chr19: 20,880,325-20,880,325 , GRCh38.p12 chr19|NW_003315962.1: 223,601-223,601 0
    nsv6130322insertion1nstd186human GRCh37 chr19: 20,926,317-20,926,358 , GRCh38.p12 chr19: 20,743,511-20,743,552 , GRCh38.p12 chr19|NW_003315962.1: 80,371-80,412 0
    nsv6129962insertion1nstd186human GRCh37 chr19: 21,101,989-21,101,989 , GRCh38.p12 chr19: 20,919,183-20,919,183 , GRCh38.p12 chr19|NW_003315962.1: 262,459-262,459 0
    nsv6127819copy number variation1nstd186human GRCh37 chr19: 21,092,647-21,092,760 , GRCh38.p12 chr19: 20,909,841-20,909,954 , GRCh38.p12 chr19|NW_003315962.1: 253,117-253,230 LOC100418992
    nsv6124044copy number variation1nstd186human GRCh37 chr19: 21,005,776-21,006,087 , GRCh38.p12 chr19: 20,822,970-20,823,281 , GRCh38.p12 chr19|NW_003315962.1: 159,753-160,054 0
    nsv5392086copy number variation3nstd186human GRCh37 chr19: 21,093,347-21,094,134 , GRCh38.p12 chr19|NW_003315962.1: 253,817-254,604 , GRCh38.p12 chr19: 20,910,541-20,911,328 LOC100418992
    nsv5391132copy number variation2nstd186human GRCh37 chr19: 21,050,098-21,050,488 , GRCh38.p12 chr19: 20,867,292-20,867,682 , GRCh38.p12 chr19|NW_003315962.1: 210,568-210,958 0
    nsv5390904copy number variation1nstd186human GRCh37 chr19: 21,156,920-21,166,017 , GRCh38.p12 chr19: 20,974,114-20,983,211 , GRCh38.p12 chr19|NW_003315962.1: 317,390-326,487 LOC112268247
    nsv5341293translocation1nstd200human GRCh37 chr19: 20,997,487-20,997,487 , GRCh37 chr9: 75,457,142-75,457,142 , GRCh38.p12 chr9: 72,842,226-72,842,226 , GRCh38.p12 chr19|NW_003315962.1: 151,654-151,654 , GRCh38.p12 chr19: 20,814,681-20,814,681 0
    nsv5340371translocation1nstd200human GRCh37 chr19: 20,620,121-20,620,121 , GRCh37 chr19: 20,953,635-20,953,635 , GRCh38.p12 chr19: 20,770,829-20,770,829 , GRCh38.p12 chr19: 20,437,315-20,437,315 , GRCh38.p12 chr19|NW_003315962.1: 107,689-107,689 LOC105372317
    nsv5339124translocation1nstd200human GRCh37 chr19: 21,207,980-21,207,980 , GRCh37 chr19: 21,203,867-21,203,867 , GRCh38.p12 chr19: 21,025,174-21,025,174 , GRCh38.p12 chr19|NW_003315962.1: 368,450-368,450 , GRCh38.p12 chr19|NW_003315962.1: 364,337-364,337 , GRCh38.p12 chr19: 21,021,061-21,021,061 ZNF430
    nsv5338967translocation1nstd200human GRCh37 chr19: 21,143,361-21,143,361 , GRCh37 chr19: 21,143,299-21,143,299 , GRCh38.p12 chr19: 20,960,493-20,960,493 , GRCh38.p12 chr19: 20,960,555-20,960,555 , GRCh38.p12 chr19|NW_003315962.1: 303,831-303,831 , GRCh38.p12 chr19|NW_003315962.1: 303,769-303,769 KRT18P40
    nsv5330550translocation1nstd200human GRCh37 chr19: 20,802,059-20,802,059 , GRCh37 chr19: 20,882,985-20,882,985 , GRCh38.p12 chr19: 20,619,253-20,619,253 , GRCh38.p12 chr19: 20,700,179-20,700,179 , GRCh38.p12 chr19|NW_003315962.1: 37,039-37,039 ZNF626
    nsv4865030copy number variation1nstd200human GRCh37 chr19: 21,176,491-21,185,134 , GRCh38.p12 chr19|NW_003315962.1: 336,961-345,604 , GRCh38.p12 chr19: 20,993,685-21,002,328 0
    nsv4865029copy number variation1nstd200human GRCh37 chr19: 21,093,347-21,094,134 , GRCh38.p12 chr19|NW_003315962.1: 253,817-254,604 , GRCh38.p12 chr19: 20,910,541-20,911,328 LOC100418992
    nsv4865028copy number variation1nstd200human GRCh37 chr19: 21,089,049-21,090,481 , GRCh38.p12 chr19: 20,906,243-20,907,675 , GRCh38.p12 chr19|NW_003315962.1: 249,519-250,951 0
    nsv4865027copy number variation1nstd200human GRCh37 chr19: 21,087,480-21,092,966 , GRCh38.p12 chr19: 20,904,674-20,910,160 , GRCh38.p12 chr19|NW_003315962.1: 247,950-253,436 LOC100418991, LOC100418992
    nsv4865026copy number variation1nstd200human GRCh37 chr19: 21,082,561-21,112,788 , GRCh38.p12 chr19: 20,899,755-20,929,982 , GRCh38.p12 chr19|NW_003315962.1: 243,031-273,258 ZNF85, LOC100418993, 3 more genes
    nsv4865025copy number variation1nstd200human GRCh37 chr19: 21,082,457-21,099,070 , GRCh38.p12 chr19: 20,899,651-20,916,264 , GRCh38.p12 chr19|NW_003315962.1: 242,927-259,540 LOC100418991, LOC100418992, 2 more genes
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