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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5315064copy number variation1nstd204human GRCh38.p13 chr8: 50,205,019-51,714,381 , GRCh37.p13 chr8: 51,117,579-52,626,941 BRIX1P1, SNTG1, 8 more genes
    nsv5249739copy number variation1nstd204human GRCh38.p13 chr8: 50,204,801-51,442,300 , GRCh37.p13 chr8: 51,117,361-52,354,860 LOC100422267, SNTG1, 8 more genes
    nsv5248946copy number variation1nstd204human GRCh38.p13 chr8: 51,433,904-51,448,819 , GRCh37.p13 chr8: 52,346,464-52,361,379 BRIX1P1, PXDNL
    nsv4825821copy number variation1nstd200human GRCh37 chr8: 51,117,589-52,626,932 , GRCh38.p12 chr8: 50,205,029-51,714,372 LOC100422267, LOC100128686, 8 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 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
    nsv4455418copy number variation1nstd102humanUncertain significance GRCh37 chr8: 51,814,887-52,659,910 , GRCh38.p12 chr8: 50,902,327-51,747,350 LOC105375831, BTF3P1, 3 more genes
    nsv4455341copy number variation1nstd102humanUncertain significance GRCh37 chr8: 50,665,945-52,739,889 , GRCh38.p12 chr8: 49,753,385-51,827,329 BTF3P1, SNTG1, 11 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
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4158715copy number variation1nstd166human GRCh37.p13 chr8: 52,185,264-52,543,829 , GRCh38.p12 chr8: 51,272,704-51,631,269 BRIX1P1, PXDNL
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 LOC105375849, RP1, 103 more genes
    nsv3923811copy number variation1nstd102humanUncertain significance GRCh37 chr8: 50,709,120-52,714,632 , GRCh38 chr8: 49,796,560-51,802,072 , NCBI36 chr8: 50,871,673-52,877,185 BTF3P1, LOC105375831, 10 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 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
    nsv3920608copy number variation1nstd102humanUncertain significance NCBI36 chr8: 50,530,318-52,746,196 , GRCh38 chr8: 49,455,206-51,671,083 , GRCh37 chr8: 50,367,765-52,583,643 LOC105375830, LOC100128686, 10 more genes
    nsv3919960copy number variation1nstd102humanUncertain significance GRCh37 chr8: 51,133,430-52,607,133 , NCBI36 chr8: 51,295,983-52,769,686 , GRCh38 chr8: 50,220,870-51,694,573 CYCSP22, LOC105375829, 8 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
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