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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7094917copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,754,127-73,754,690 , GRCh38.p12 chr17: 75,758,046-75,758,609 GALK1, ITGB4
    nsv7073965inversion1nstd229human GRCh38 chr17: 75,577,011-75,829,469 , GRCh37.p13 chr17: 73,573,092-73,825,550 UNK, SMIM5, 10 more genes
    nsv7062058inversion1nstd229human GRCh38 chr17: 75,576,996-75,829,470 , GRCh37.p13 chr17: 73,573,077-73,825,551 UNC13D, SMIM5, 10 more genes
    nsv6996054copy number variation1nstd229human GRCh38 chr17: 75,739,901-75,740,900 , GRCh37.p13 chr17: 73,735,982-73,736,981 ITGB4
    nsv6994027copy number variation1nstd229human GRCh38 chr17: 75,738,056-75,741,892 , GRCh37.p13 chr17: 73,734,137-73,737,973 ITGB4
    nsv6989185copy number variation1nstd229human GRCh38 chr17: 75,743,256-75,743,447 , GRCh37.p13 chr17: 73,739,337-73,739,528 ITGB4
    nsv6985706copy number variation1nstd229human GRCh38 chr17: 75,748,801-75,758,700 , GRCh37.p13 chr17: 73,744,882-73,754,781 GALK1, ITGB4
    nsv6984413copy number variation1nstd229human GRCh38 chr17: 75,743,862-75,748,839 , GRCh37.p13 chr17: 73,739,943-73,744,920 ITGB4
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983209copy number variation1nstd229human GRCh38 chr17: 75,729,714-75,830,368 , GRCh37.p13 chr17: 73,725,795-73,826,449 UNC13D, MIR4738, 4 more genes
    nsv6978932copy number variation1nstd229human GRCh38 chr17: 75,752,577-75,754,574 , GRCh37.p13 chr17: 73,748,658-73,750,655 ITGB4
    nsv6589966inversion1nstd223human GRCh38 chr17: 75,576,986-75,829,587 , GRCh37.p13 chr17: 73,573,067-73,825,668 RECQL5, MIR4738, 10 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6533255copy number variation1nstd223human GRCh38 chr17: 75,715,801-75,746,496 , GRCh37.p13 chr17: 73,711,881-73,742,577 ITGB4
    nsv6532698copy number variation1nstd223human GRCh38 chr17: 75,734,570-75,735,119 , GRCh37.p13 chr17: 73,730,651-73,731,200 ITGB4
    nsv6525784copy number variation1nstd223human GRCh38 chr17: 75,723,383-75,726,611 , GRCh37.p13 chr17: 73,719,463-73,722,691 ITGB4
    nsv6315207copy number variation1nstd102humanPathogenic GRCh38 chr17: 75,749,003-75,751,286 , GRCh37 chr17: 73,745,084-73,747,367 ITGB4
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6310408copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,754,127-73,761,239 , GRCh38.p12 chr17: 75,758,046-75,765,158 ITGB4, GALK1
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