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Items: 1 to 20 of 1047

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130961insertion1nstd186human GRCh37 chr16: 542,441-542,490 , GRCh38.p12 chr16: 492,441-492,490 , GRCh38.p12 chr16|NT_187610.1: 94,503-94,558 LOC107987417, RAB11FIP3
    nsv6121944copy number variation1nstd186human GRCh37 chr16: 542,360-542,541 , GRCh38.p12 chr16: 492,360-492,541 RAB11FIP3
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5978960inversion1nstd209human GRCh38 chr16: 435,702-437,576 , GRCh37.p13 chr16: 485,702-487,576 RAB11FIP3
    nsv5970637insertion1nstd209human GRCh38 chr16: 433,137-433,137 , GRCh37.p13 chr16: 483,137-483,137 RAB11FIP3
    nsv5969473inversion1nstd209human GRCh38 chr16: 460,657-462,313 , GRCh37.p13 chr16: 510,657-512,313 RAB11FIP3
    nsv5945795copy number variation1nstd209human GRCh38 chr16: 492,681-494,360 , GRCh37.p13 chr16: 542,681-544,360 RAB11FIP3
    nsv5943567copy number variation1nstd209human GRCh38 chr16: 448,072-448,357 , GRCh37.p13 chr16: 498,072-498,357 RAB11FIP3
    nsv5939794copy number variation1nstd209human GRCh38 chr16: 435,780-437,894 , GRCh37.p13 chr16: 485,780-487,894 RAB11FIP3
    nsv5938171copy number variation1nstd209human GRCh38 chr16: 518,485-518,617 , GRCh37.p13 chr16: 568,485-568,617 RAB11FIP3
    nsv5937862copy number variation1nstd209human GRCh38 chr16: 435,754-438,561 , GRCh37.p13 chr16: 485,754-488,561 RAB11FIP3
    nsv5935118copy number variation1nstd209human GRCh38 chr16: 453,033-453,352 , GRCh37.p13 chr16: 503,033-503,352 RAB11FIP3
    nsv5934089copy number variation1nstd209human GRCh38 chr16: 460,876-460,978 , GRCh37.p13 chr16: 510,876-510,978 RAB11FIP3
    nsv5932337copy number variation1nstd209human GRCh38 chr16: 435,200-437,566 , GRCh37.p13 chr16: 485,200-487,566 RAB11FIP3
    nsv5932044copy number variation1nstd209human GRCh38 chr16: 480,776-481,086 , GRCh37.p13 chr16: 530,776-531,086 RAB11FIP3
    nsv5929715copy number variation1nstd209human GRCh38 chr16: 448,353-448,485 , GRCh37.p13 chr16: 498,353-498,485 RAB11FIP3
    nsv5928758copy number variation1nstd209human GRCh38 chr16: 477,032-478,475 , GRCh37.p13 chr16: 527,032-528,475 RAB11FIP3
    nsv5927793copy number variation1nstd209human GRCh38 chr16: 487,370-494,147 , GRCh37.p13 chr16: 537,370-544,147 RAB11FIP3
    nsv5887289copy number variation1nstd209human GRCh38 chr16: 437,514-438,613 , GRCh37.p13 chr16: 487,514-488,613 RAB11FIP3
    nsv5872732copy number variation1nstd209human GRCh38 chr16: 431,482-437,013 , GRCh37.p13 chr16: 481,482-487,013 RAB11FIP3
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