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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562272inversion1nstd206human GRCh38 chr8: 109,970,585-109,970,728 , GRCh37.p13 chr8: 110,982,814-110,982,957 KCNV1
    nsv5549980insertion1nstd206human GRCh38 chr8: 109,970,708-109,970,708 , GRCh37.p13 chr8: 110,982,937-110,982,937 KCNV1
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4729071copy number variation1nstd102humanPathogenic GRCh37 chr8: 108,421,573-123,429,638 , GRCh38.p12 chr8: 107,409,345-122,417,399 RN7SL396P, LOC107986970, 124 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455916copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,437,051-114,170,843 , GRCh38.p12 chr8: 103,424,823-113,158,614 LOC105375688, DPYS, 82 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4341151sequence alteration1nstd166human GRCh37.p13 chr8: 110,982,592-110,982,943 , GRCh38.p12 chr8: 109,970,363-109,970,714 KCNV1
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4164885copy number variation1nstd166human GRCh37.p13 chr8: 110,954,641-110,982,775 , GRCh38.p12 chr8: 109,942,412-109,970,546 KCNV1
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922364copy number variation1nstd102humanUncertain significance GRCh37 chr8: 108,368,406-111,925,723 , GRCh38 chr8: 107,356,178-110,913,494 , NCBI36 chr8: 108,437,582-111,994,899 LOC100420748, LOC644335, 29 more genes
    nsv3919841copy number variation1nstd102humanPathogenic GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824 LY6S-AS1, LOC107984017, 911 more genes
    nsv3919636copy number variation1nstd102humanPathogenic NCBI36 chr8: 101,948,747-146,266,575 , GRCh38 chr8: 100,867,343-145,070,385 , GRCh37 chr8: 101,879,571-146,295,771 RSPO2, MTND2P35, 592 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3916978copy number variation1nstd102humanPathogenic GRCh38 chr8: 86,300,584-137,022,587 , NCBI36 chr8: 87,381,929-138,104,012 , GRCh37 chr8: 87,312,813-138,034,830 MIR5194, TRS-AGA2-5, 601 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 more genes
    nsv3916438copy number variation1nstd102humanPathogenic GRCh37 chr8: 46,942,962-140,297,737 , NCBI36 chr8: 47,062,127-140,366,919 , GRCh38 chr8: 46,031,340-139,285,494 NDUFS5P6, LINC01289, 1152 more genes
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