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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6996451copy number variation1nstd229human GRCh38 chr16: 53,410,901-53,448,800 , GRCh37.p13 chr16: 53,444,813-53,482,712 RNU6-1153P, RBL2
    nsv6992861copy number variation1nstd229human GRCh38 chr16: 53,427,243-53,433,734 , GRCh37.p13 chr16: 53,461,155-53,467,646 RBL2
    nsv6981038copy number variation1nstd229human GRCh38 chr16: 53,471,273-53,475,537 , GRCh37.p13 chr16: 53,505,185-53,509,449 RBL2
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6578074inversion1nstd223human GRCh38 chr16: 53,439,931-53,440,971 , GRCh37.p13 chr16: 53,473,843-53,474,883 RBL2
    nsv6513873copy number variation1nstd223human GRCh38 chr16: 53,440,701-53,442,000 , GRCh37.p13 chr16: 53,474,613-53,475,912 RNU6-1153P, RBL2
    nsv6497363copy number variation1nstd223human GRCh38 chr16: 53,472,001-53,473,900 , GRCh37.p13 chr16: 53,505,913-53,507,812 RBL2
    nsv6497337copy number variation1nstd223human GRCh38 chr16: 53,477,701-53,478,400 , GRCh37.p13 chr16: 53,511,613-53,512,312 RBL2
    nsv6496448copy number variation1nstd223human GRCh38 chr16: 53,438,952-53,440,178 , GRCh37.p13 chr16: 53,472,864-53,474,090 RBL2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6290225copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,445,684-53,451,836 , GRCh37 chr16: 53,479,596-53,485,748 RBL2
    nsv6250284mobile element insertion1nstd215human GRCh38 chr16: 53,478,561-53,478,561 , GRCh37.p13 chr16: 53,512,473-53,512,473 RBL2
    nsv6250283mobile element insertion1nstd215human GRCh38 chr16: 53,465,846-53,465,846 , GRCh37.p13 chr16: 53,499,758-53,499,758 RBL2
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6084278insertion1nstd212human GRCh38 chr16: 53,447,689-53,447,689 , GRCh37.p13 chr16: 53,481,601-53,481,601 RBL2
    nsv5979275insertion1nstd209human GRCh38 chr16: 53,457,258-53,457,258 , GRCh37.p13 chr16: 53,491,170-53,491,170 RBL2
    nsv5887514copy number variation1nstd209human GRCh38 chr16: 53,472,312-53,473,611 , GRCh37.p13 chr16: 53,506,224-53,507,523 RBL2
    nsv5695006mobile element insertion1nstd211human GRCh38 chr16: 53,465,846-53,465,846 , GRCh37.p13 chr16: 53,499,758-53,499,758 RBL2
    nsv5519586copy number variation1nstd206human GRCh38 chr16: 53,426,293-53,440,236 , GRCh37.p13 chr16: 53,460,205-53,474,148 RBL2
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