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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3109784copy number variation2nstd37humanUncertain significance, Likely benign GRCh37 (hg19) chr13: 61,660,181-63,785,757 , GRCh38 (hg38) chr13: 61,086,047-63,211,624 , NCBI36 (hg18) chr13: 60,558,182-62,683,758 MIR3169, LINC00358, 5 more genes
    esv4010042copy number variation1estd232humanPathogenic GRCh37 (hg19) chr11: 21,586,131-33,168,232 , GRCh38 (hg38) chr11: 21,564,585-33,146,686 CCDC179, DCDC5, 54 more genes
    nsv2778482copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr8: 11,362,682-11,709,476 , GRCh38 (hg38) chr8: 11,505,173-11,851,967 , NCBI36 (hg18) chr8: 11,400,091-11,746,885 SNORA99, CTSB, 6 more genes
    nsv2777827copy number variation1nstd37humanLikely benign GRCh37 (hg19) chr3: 160,955,748-161,267,703 , GRCh38 (hg38) chr3: 161,237,960-161,549,915 , NCBI36 (hg18) chr3: 162,438,442-162,750,397 LINC02067, OTOL1, 2 more genes
    nsv2777822copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 76,061,144-102,429,112 , GRCh38 (hg38) chr15: 75,768,803-101,888,909 , NCBI36 (hg18) chr15: 73,848,199-100,246,635 UBE2Q2P3, GOLGA6L3, 246 more genes
    nsv2776670copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr1: 3,683,105-3,712,456 , GRCh38 (hg38) chr1: 3,766,541-3,795,892 , NCBI36 (hg18) chr1: 3,672,965-3,702,316 CCDC27, SMIM1, 1 more genes
    nsv2775904copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr20: 61,602,977-62,450,998 , GRCh38 (hg38) chr20: 62,971,625-63,819,645 , NCBI36 (hg18) chr20: 61,073,422-61,921,442 LINC00029, LINC01056, 33 more genes
    nsv2775103copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr12: 131,390,795-132,104,151 , GRCh38 (hg38) chr12: 130,906,250-131,619,606 , NCBI36 (hg18) chr12: 129,956,748-130,670,104 ADGRD1-AS1, LINC02415, 3 more genes
    nsv2774599copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr1: 103,480,265-105,286,199 , GRCh38 (hg38) chr1: 103,014,709-104,743,577 , NCBI36 (hg18) chr1: 103,252,853-105,087,722 COL11A1, AMY1A, 6 more genes
    nsv2773959copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr12: 122,614,468-123,019,270 , GRCh38 (hg38) chr12: 122,145,577-122,534,723 , NCBI36 (hg18) chr12: 121,180,421-121,585,223 CLIP1-AS1, MLXIP, 9 more genes
    nsv2773458copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr8: 114,132,971-114,357,413 , GRCh38 (hg38) chr8: 113,120,742-113,345,184 , NCBI36 (hg18) chr8: 114,202,147-114,426,589 CSMD3
    nsv2772709copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr2: 86,285,942-86,519,246 , GRCh38 (hg38) chr2: 86,058,819-86,292,123 , NCBI36 (hg18) chr2: 86,139,453-86,372,757 MIR4779, IMMT, 5 more genes
    nsv2771728copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr15: 25,196,959-25,200,389 , GRCh38 (hg38) chr15: 24,951,812-24,955,242 , NCBI36 (hg18) chr15: 22,748,052-22,751,482 SNRPN, SNURF
    nsv2771718copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 140,533,290-140,716,973 , GRCh38 (hg38) chr9: 137,638,838-137,822,521 , NCBI36 (hg18) chr9: 139,653,111-139,836,794 EHMT1-IT1, EHMT1
    nsv2770576copy number variation2nstd37humanUncertain significance GRCh37 (hg19) chr19: 56,874,577-57,183,789 , GRCh38 (hg38) chr19: 56,363,208-56,672,421 , NCBI36 (hg18) chr19: 61,566,389-61,875,601 ZNF667-AS1, ZIM2-AS1, 11 more genes
    nsv2770178copy number variation2nstd37humanUncertain significance, Likely benign GRCh37 (hg19) chr9: 611,150-694,567 , GRCh38 (hg38) chr9: 611,150-694,567 , NCBI36 (hg18) chr9: 601,150-684,567 KANK1
    nsv2770020copy number variation1nstd37humanLikely benign GRCh37 (hg19) chr15: 28,946,433-30,386,398 , GRCh38.p2 chr15|NT_187660.1: 977,075-2,379,399 , GRCh38.p2 chr15|NW_011332701.1: 863,289-2,266,915 , GRCh38 (hg38) chr15: 28,701,287-30,094,195 , NCBI36 (hg18) chr15: 26,745,474-28,173,690 FAM189A1, APBA2, 5 more genes
    nsv2769549copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr18: 136,226-21,657,790 , GRCh38 (hg38) chr18: 136,226-24,077,826 , NCBI36 (hg18) chr18: 126,226-19,911,788 GATA6-AS1, LINC01387, 134 more genes
    nsv2769110copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr10: 70,525,750-70,775,715 , GRCh38 (hg38) chr10: 68,765,993-69,015,959 , NCBI36 (hg18) chr10: 70,195,756-70,445,721 STOX1, KIF1BP, 3 more genes
    esv3897364inversion1estd223cow Bos_taurus_UMD_3.1 chr18: 16,225,226-23,179,057 , Btau_5.0.1 chr18: 16,271,938-23,236,347 , Bos_taurus_UMD_3.1.1 chr18: 16,225,226-23,179,057 TRNAE-CUC, TRNAC-ACA, 27 more genes
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