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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095218copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,411,496-50,766,697 , GRCh38.p12 chr19: 49,908,239-50,263,440 SNAR-A6, SNAR-A14, 23 more genes
    nsv7077743inversion1nstd229human GRCh38 chr19: 49,995,881-50,059,283 , GRCh37.p13 chr19: 50,499,138-50,562,540 ZNF473CR, LOC100287477, 2 more genes
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7073780inversion1nstd229human GRCh38 chr19: 50,057,270-50,232,309 , GRCh37.p13 chr19: 50,560,527-50,735,566 LOC100287477, SNAR-A4, 15 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7013373copy number variation1nstd229human GRCh38 chr19: 49,962,038-50,073,196 , GRCh37.p13 chr19: 50,465,295-50,576,453 VRK3, LOC100287477, 3 more genes
    nsv7012129copy number variation1nstd229human GRCh38 chr19: 50,051,401-50,057,700 , GRCh37.p13 chr19: 50,554,658-50,560,957 LOC100287477, ZNF473CR
    nsv7001279copy number variation1nstd229human GRCh38 chr19: 50,050,501-50,057,700 , GRCh37.p13 chr19: 50,553,758-50,560,957 ZNF473CR, LOC100287477
    nsv6598837inversion1nstd223human GRCh38 chr19: 50,057,567-50,058,143 , GRCh37.p13 chr19: 50,560,824-50,561,400 LOC100287477, ZNF473CR
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6529768copy number variation1nstd223human GRCh38 chr19: 50,048,023-50,049,923 , GRCh37.p13 chr19: 50,551,280-50,553,180 ZNF473, ZNF473CR
    nsv6527316copy number variation1nstd223human GRCh38 chr19: 50,050,901-50,058,200 , GRCh37.p13 chr19: 50,554,158-50,561,457 ZNF473CR, LOC100287477
    nsv6519449copy number variation1nstd223human GRCh38 chr19: 50,053,901-50,054,700 , GRCh37.p13 chr19: 50,557,158-50,557,957 ZNF473CR
    nsv6519299copy number variation1nstd223human GRCh38 chr19: 50,055,201-50,057,700 , GRCh37.p13 chr19: 50,558,458-50,560,957 ZNF473CR, LOC100287477
    nsv6519120copy number variation1nstd223human GRCh38 chr19: 50,055,424-50,063,758 , GRCh37.p13 chr19: 50,558,681-50,567,015 ZNF473CR, LOC100287477
    nsv6516773copy number variation1nstd223human GRCh38 chr19: 50,018,966-50,089,286 , GRCh37.p13 chr19: 50,522,223-50,592,543 VRK3, LOC100287477, 2 more genes
    nsv6314099copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,355,646-50,552,140 , GRCh38.p12 chr19: 49,852,389-50,048,883 IL4I1, SIGLEC11, 14 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
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