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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131074insertion1nstd186human GRCh37 chr19: 47,220,476-47,220,520 , GRCh38.p12 chr19: 46,717,219-46,717,263 PRKD2, LOC107987269
    nsv5947148copy number variation1nstd209human GRCh38 chr19: 46,711,653-46,711,874 , GRCh37.p13 chr19: 47,214,910-47,215,131 PRKD2
    nsv5945014copy number variation1nstd209human GRCh38 chr19: 46,686,609-46,686,907 , GRCh37.p13 chr19: 47,189,866-47,190,164 PRKD2, RN7SL364P
    nsv5940467copy number variation1nstd209human GRCh38 chr19: 46,684,719-46,685,014 , GRCh37.p13 chr19: 47,187,976-47,188,271 PRKD2
    nsv5929369copy number variation1nstd209human GRCh38 chr19: 46,680,748-46,680,997 , GRCh37.p13 chr19: 47,184,005-47,184,254 PRKD2
    nsv5929323copy number variation1nstd209human GRCh38 chr19: 46,712,210-46,712,506 , GRCh37.p13 chr19: 47,215,467-47,215,763 PRKD2
    nsv5929296copy number variation1nstd209human GRCh38 chr19: 46,694,804-46,696,486 , GRCh37.p13 chr19: 47,198,061-47,199,743 PRKD2
    nsv5868476copy number variation1nstd209human GRCh38 chr19: 46,694,794-46,696,593 , GRCh37.p13 chr19: 47,198,051-47,199,850 PRKD2
    nsv5554122sequence alteration1nstd206human GRCh38 chr19: 46,683,957-46,688,032 , GRCh37.p13 chr19: 47,187,214-47,191,289 PRKD2, RN7SL364P
    nsv5547398insertion1nstd206human GRCh38 chr19: 46,717,219-46,717,263 , GRCh37.p13 chr19: 47,220,476-47,220,520 PRKD2, LOC107987269
    nsv5538043insertion1nstd206human GRCh38 chr19: 46,715,777-46,715,824 , GRCh37.p13 chr19: 47,219,034-47,219,081 PRKD2, LOC107987269
    nsv5534146insertion1nstd206human GRCh38 chr19: 46,688,019-46,688,019 , GRCh37.p13 chr19: 47,191,276-47,191,276 RN7SL364P, PRKD2
    nsv5530384copy number variation1nstd206human GRCh38 chr19: 46,686,364-46,686,557 , GRCh37.p13 chr19: 47,189,621-47,189,814 PRKD2
    nsv5020780copy number variation1nstd200human GRCh38 chr19: 46,680,572-46,681,196 , GRCh37.p13 chr19: 47,183,829-47,184,453 PRKD2
    nsv4682791copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,109,074-47,260,205 , GRCh38.p12 chr19: 46,605,817-46,756,948 DACT3, FKRP, 9 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4540991insertion1nstd166human GRCh37.p13 chr19: 47,219,030-47,219,030 , GRCh38.p12 chr19: 46,715,773-46,715,773 PRKD2, LOC107987269
    nsv4502564mobile element insertion1nstd166human GRCh37.p13 chr19: 47,181,465-47,181,465 , GRCh38.p12 chr19: 46,678,208-46,678,208 PRKD2
    nsv4500523mobile element insertion1nstd166human GRCh37.p13 chr19: 47,208,082-47,208,082 , GRCh38.p12 chr19: 46,704,825-46,704,825 PRKD2
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