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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4961958copy number variation1nstd200human GRCh38 chr8: 112,521,112-112,940,227 , GRCh37.p13 chr8: 113,533,341-113,952,456 CSMD3, RPL30P16, 1 more genes
    nsv4961952copy number variation1nstd200human GRCh38 chr8: 112,369,579-113,295,992 , GRCh37.p13 chr8: 113,381,808-114,308,221 MIR2053, CSMD3, 2 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
    nsv4675222copy number variation1nstd102humanPathogenic GRCh37 chr8: 111,514,791-123,192,373 , GRCh38.p12 chr8: 110,502,562-122,180,134 LOC105375723, CSMD3, 93 more genes
    nsv4613706copy number variation1nstd183human GRCh37 chr8: 113,652,365-113,825,183 , GRCh38.p12 chr8: 112,640,136-112,812,954 CSMD3, MIR2053
    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
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4172163copy number variation1nstd166human GRCh37.p13 chr8: 113,386,389-113,734,264 , GRCh38.p12 chr8: 112,374,160-112,722,035 CSMD3, RPL30P16, 1 more genes
    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
    nsv3922607copy number variation1nstd102humanUncertain significance GRCh37 chr8: 113,618,413-113,719,181 , GRCh38 chr8: 112,606,184-112,706,952 CSMD3, MIR2053
    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
    nsv3919824copy number variation1nstd102humanUncertain significance NCBI36 chr8: 113,655,006-114,048,251 , GRCh37 chr8: 113,585,830-113,979,075 , GRCh38 chr8: 112,573,601-112,966,846 MIR2053, CSMD3
    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
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