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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3907075copy number variation1nstd102humanBenign GRCh37 chr11: 65,349,504-65,363,063 , GRCh38.p12 chr11: 65,582,033-65,595,592 KCNK7, EHBP1L1
    nsv3894865copy number variation1nstd102humanBenign GRCh37 chr11: 65,348,529-65,361,309 , GRCh38.p12 chr11: 65,581,058-65,593,838 KCNK7, EHBP1L1
    nsv3905509copy number variation1nstd102humanBenign GRCh37 chr11: 65,351,019-65,362,975 , GRCh38.p12 chr11: 65,583,548-65,595,504 KCNK7, EHBP1L1
    nsv3900051copy number variation1nstd102humanBenign GRCh37 chr11: 65,351,159-65,362,975 , GRCh38.p12 chr11: 65,583,688-65,595,504 KCNK7, EHBP1L1
    nsv3890725copy number variation1nstd102humanBenign GRCh37 chr11: 65,351,159-65,361,309 , GRCh38.p12 chr11: 65,583,688-65,593,838 KCNK7, EHBP1L1
    nsv3890921copy number variation1nstd102humanBenign GRCh37 chr11: 65,351,779-65,361,309 , GRCh38.p12 chr11: 65,584,308-65,593,838 KCNK7, EHBP1L1
    nsv3906770copy number variation1nstd102humanBenign GRCh37 chr11: 65,338,400-65,361,765 , GRCh38.p12 chr11: 65,570,929-65,594,294 KCNK7, EHBP1L1, 2 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 KCNK7, FAUP4, 2031 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 KCNK7, SF3B2, 124 more genes
    nsv7093933copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 65,325,080-65,639,825 , GRCh38.p12 chr11: 65,557,609-65,872,354 KCNK7, ZNRD2-DT, 22 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 KCNK7, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 KCNK7, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 KCNK7, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 KCNK7, PYGM, 2125 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 KCNK7, SNORD13F, 141 more genes
    nsv3902272copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787 KCNK7, ACTN3, 157 more genes
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 KCNK7, ARL2, 117 more genes
    nsv3903507copy number variation1nstd102humanBenign GRCh37 chr11: 65,347,930-65,421,892 , GRCh38.p12 chr11: 65,580,459-65,654,421 KCNK7, MIR4690, 6 more genes
    nsv3893576copy number variation1nstd102humanBenign GRCh37 chr11: 65,144,318-65,373,538 , GRCh38.p12 chr11: 65,376,847-65,606,067 KCNK7, SNRPGP19, 16 more genes
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 KCNK7, CNIH2, 95 more genes
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