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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4962744copy number variation1nstd200human GRCh38 chr8: 144,790,122-144,790,203 , GRCh37.p13 chr8: 146,015,507-146,015,588 RPL8, MIR6850
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4613322copy number variation1nstd183human GRCh37 chr8: 146,017,442-146,017,724 , GRCh38.p12 chr8: 144,792,057-144,792,339 MIR6850, RPL8
    nsv4600813copy number variation1nstd183human GRCh37 chr8: 146,017,096-146,017,807 , GRCh38.p12 chr8: 144,791,711-144,792,422 RPL8, MIR6850
    nsv4457078copy number variation1nstd102humanPathogenic GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385 GSDMD, MROH1, 181 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 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
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4456582copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,939,952-146,050,283 , GRCh38.p12 chr8: 144,714,567-144,824,898 ZNF34, LOC100996662, 8 more genes
    nsv4455561copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,897,164-146,109,987 , GRCh38.p12 chr8: 144,671,779-144,884,602 ZNF517, ZNF34, 12 more genes
    nsv4455524copy number variation1nstd102humanPathogenic GRCh37 chr8: 136,059,859-146,295,771 , GRCh38.p12 chr8: 135,047,616-145,070,385 LINC00051, LOC107986982, 197 more genes
    nsv4455260copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,190,206-146,295,771 , GRCh38.p12 chr8: 143,108,789-145,070,385 COMMD5, RHPN1-AS1, 113 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
    nsv4157242copy number variation1nstd166human GRCh37.p13 chr8: 145,966,559-146,033,905 , GRCh38.p12 chr8: 144,741,174-144,808,520 RPL8, ZNF34, 7 more genes
    nsv3924568copy number variation1nstd102humanPathogenic NCBI36 chr8: 131,720,610-146,264,902 , GRCh38 chr8: 130,639,182-145,068,712 , GRCh37 chr8: 131,651,428-146,294,098 MAFA-AS1, DENND3-AS1, 244 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
    nsv3922201copy number variation1nstd102humanPathogenic NCBI36 chr8: 129,302,340-146,245,639 , GRCh38 chr8: 128,220,912-145,049,449 , GRCh37 chr8: 129,233,158-146,274,835 CYP11B2, SLC45A4-AS1, 261 more genes
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