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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075434inversion1nstd229human GRCh38 chr19: 20,528,960-23,693,763 , GRCh37.p13 chr19: 20,845,947-23,876,565 LOC105372339, RPL36AP51, 124 more genes
    nsv7017948copy number variation1nstd229human GRCh38 chr19: 22,288,891-23,480,362 , GRCh37.p13 chr19: 22,471,693-23,663,164 ZNF91, RPL34P33, 49 more genes
    nsv7015463copy number variation1nstd229human GRCh38 chr19: 23,287,201-23,290,600 , GRCh37.p13 chr19: 23,470,003-23,473,402 VN1R91P, VN1R90P
    nsv7009684copy number variation1nstd229human GRCh38 chr19: 23,075,857-23,478,376 , GRCh37.p13 chr19: 23,258,659-23,661,178 VN1R91P, ZNF91, 15 more genes
    nsv7009200copy number variation1nstd229human GRCh38 chr19: 23,287,187-23,290,620 , GRCh37.p13 chr19: 23,469,989-23,473,422 VN1R91P, VN1R90P
    nsv7006469copy number variation1nstd229human GRCh38 chr19: 23,205,508-23,309,246 , GRCh37.p13 chr19: 23,388,310-23,492,048 ZNF91, IPO5P1, 4 more genes
    nsv7003854copy number variation1nstd229human GRCh38 chr19: 23,164,522-23,329,944 , GRCh37.p13 chr19: 23,347,324-23,512,746 LOC107985285, IPO5P1, 5 more genes
    nsv6637478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 23,217,767-23,956,831 , GRCh38.p12 chr19: 23,034,965-23,774,029 ZNF681, IPO5P1, 27 more genes
    nsv6624453copy number variation1nstd224human GRCh37 chr19: 23,150,326-23,566,038 , GRCh38.p12 chr19: 22,967,524-23,383,236 ZNF724, ZNF730, 16 more genes
    nsv6599769inversion1nstd223human GRCh38 chr19: 21,518,661-23,675,522 , GRCh37.p13 chr19: 21,701,463-23,858,324 , ZNF43, 86 more genes
    nsv6597726inversion1nstd223human GRCh38 chr19: 22,434,951-23,689,752 , GRCh37.p13 chr19: 22,617,753-23,872,554 ZNF91, LOC100419307, 52 more genes
    nsv6595620inversion1nstd223human GRCh38 chr19: 20,546,381-23,697,523 , GRCh37.p13 chr19: 20,845,947-23,880,325 , MTDHP3, 125 more genes
    nsv6526298copy number variation1nstd223human GRCh38 chr19: 22,901,232-23,494,651 , GRCh37.p13 chr19: 23,084,034-23,677,453 LOC100419307, LINC01224, 22 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133695copy number variation1nstd213human GRCh37 chr19: 23,340,000-23,480,001 , GRCh38.p12 chr19: 23,157,198-23,297,199 ZNF724, IPO5P1, 3 more genes
    nsv6133402copy number variation1nstd213human GRCh37 chr19: 19,150,000-24,140,001 , GRCh38.p12 chr19: 19,039,191-23,957,199 , NCAN, 199 more genes
    nsv6133401copy number variation1nstd213human GRCh37 chr19: 19,110,000-24,140,001 , GRCh38.p12 chr19: 18,999,191-23,957,199 , NCAN, 200 more genes
    nsv6110465inversion1nstd212human GRCh38 chr19: 21,574,056-23,425,178 , GRCh37.p13 chr19: 21,756,858-23,607,980 , ZNF43, 76 more genes
    nsv5967948inversion1nstd209human GRCh38 chr19: 22,806,402-23,350,599 , GRCh37.p13 chr19: 22,989,204-23,533,401 ZNF91, SNX6P1, 18 more genes
    nsv5530175copy number variation1nstd206human GRCh38 chr19: 22,813,931-23,470,653 , GRCh37.p13 chr19: 22,996,733-23,653,455 VN1R92P, ZNF730, 23 more genes
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