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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078064inversion1nstd229human GRCh38 chr11: 89,591,780-90,101,854 , GRCh37.p13 chr11: 89,324,948-89,835,022 TRIM49D2, ANKRD33BP8, 25 more genes
    nsv7076395inversion1nstd229human GRCh38 chr11: 89,372,299-90,049,222 , GRCh37.p13 chr11: 89,105,467-89,782,390 ANKRD33BP7, TRIM53AP, 23 more genes
    nsv7072301inversion1nstd229human GRCh38 chr11: 89,705,504-90,174,109 , GRCh37.p13 chr11: 89,438,672-89,907,277 TRIM77, LOC642579, 24 more genes
    nsv7072045inversion1nstd229human GRCh38 chr11: 89,933,609-90,162,412 , GRCh37.p13 chr11: 89,666,777-89,895,580 TRIM64EP, LOC100128800, 9 more genes
    nsv7071690inversion1nstd229human GRCh38 chr11: 89,575,988-90,302,831 , GRCh37.p13 chr11: 89,309,156-90,035,999 TRIM64, UBTFL2, 30 more genes
    nsv7070364inversion1nstd229human GRCh38 chr11: 89,719,573-90,103,234 , GRCh37.p13 chr11: 89,452,741-89,836,402 TRIM64EP, LOC100128800, 22 more genes
    nsv7069320inversion1nstd229human GRCh38 chr11: 89,699,356-90,095,271 , GRCh37.p13 chr11: 89,432,524-89,828,439 ANKRD33BP8, TRIM49D2, 24 more genes
    nsv7067052inversion1nstd229human GRCh38 chr11: 89,742,472-90,098,744 , GRCh37.p13 chr11: 89,475,640-89,831,912 MTND1P35, LOC100128800, 21 more genes
    nsv7065103inversion1nstd229human GRCh38 chr11: 89,653,193-90,071,282 , GRCh37.p13 chr11: 89,386,361-89,804,450 MTND1P35, FOLH1B, 24 more genes
    nsv7064296inversion1nstd229human GRCh38 chr11: 89,450,688-90,111,328 , GRCh37.p13 chr11: 89,183,856-89,844,496 TRIM49D2, UBTFL10, 26 more genes
    nsv7063811inversion1nstd229human GRCh38 chr11: 89,755,227-90,100,774 , GRCh37.p13 chr11: 89,488,395-89,833,942 LOC100128800, TRIM49, 20 more genes
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv7059248inversion1nstd229human GRCh38 chr11: 89,584,468-90,127,453 , GRCh37.p13 chr11: 89,317,636-89,860,621 LOC100128800, TRIM77, 26 more genes
    nsv6914121copy number variation1nstd229human GRCh38 chr11: 89,708,489-94,988,932 , GRCh37.p13 chr11: 89,441,657-94,611,845 SNORA40, PIWIL4-AS1, 89 more genes
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6903114copy number variation1nstd229human GRCh38 chr11: 89,920,746-90,130,142 , GRCh37.p13 chr11: 89,653,914-89,863,310 LOC642579, TRIM51EP, 11 more genes
    nsv6637691copy number variation1nstd102humanUncertain significance GRCh37 chr11: 89,474,818-89,887,082 , GRCh38.p12 chr11: 89,741,650-90,153,914 LOC100128800, TRIM53BP, 22 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6621280copy number variation1nstd224human GRCh37 chr11: 89,548,036-89,902,531 , GRCh38.p12 chr11: 89,814,868-90,169,363 TRIM51EP, MTND1P35, 18 more genes
    nsv6621279copy number variation1nstd224human GRCh37 chr11: 89,420,607-89,768,564 , GRCh38.p12 chr11: 89,687,439-90,035,396 UBTFL2, TRIM77, 22 more genes
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