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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112741copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr8: 98,084,302-98,130,649 , GRCh37 chr8: 99,096,530-99,142,877 RIDA, POP1, 1 more genes
    nsv5703111mobile element insertion2nstd211human GRCh38 chr8: 98,124,899-98,124,899 , GRCh37.p13 chr8: 99,137,127-99,137,127 POP1
    nsv5542010insertion1nstd206human GRCh38 chr8: 98,124,899-98,124,950 , GRCh37.p13 chr8: 99,137,127-99,137,178 POP1
    nsv5486531copy number variation1nstd206human GRCh38 chr8: 98,155,455-98,155,788 , GRCh37.p13 chr8: 99,167,683-99,168,016 POP1
    nsv5481616copy number variation1nstd206human GRCh38 chr8: 98,121,661-98,122,032 , GRCh37.p13 chr8: 99,133,889-99,134,260 POP1
    nsv5479035copy number variation1nstd206human GRCh38 chr8: 98,128,829-98,129,649 , GRCh37.p13 chr8: 99,141,057-99,141,877 POP1
    nsv5474054copy number variation1nstd206human GRCh38 chr8: 98,116,014-98,116,075 , GRCh37.p13 chr8: 99,128,242-99,128,303 RIDA, POP1
    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
    nsv4961433copy number variation1nstd200human GRCh38 chr8: 98,151,241-98,155,605 , GRCh37.p13 chr8: 99,163,469-99,167,833 POP1
    nsv4961432copy number variation1nstd200human GRCh38 chr8: 98,128,829-98,129,649 , GRCh37.p13 chr8: 99,141,057-99,141,877 POP1
    nsv4829198copy number variation1nstd200human GRCh37 chr8: 98,998,960-99,500,533 , GRCh38.p12 chr8: 97,986,732-98,488,305 , RPL30, 16 more genes
    nsv4822584copy number variation1nstd200human GRCh37 chr8: 99,141,057-99,141,877 , GRCh38.p12 chr8: 98,128,829-98,129,649 POP1
    nsv4822583copy number variation1nstd200human GRCh37 chr8: 99,135,945-99,136,690 , GRCh38.p12 chr8: 98,123,717-98,124,462 POP1
    nsv4680662copy number variation1nstd189human GRCh37.p13 chr8: 98,986,034-99,193,231 , GRCh38.p12 chr8: 97,973,806-98,181,003 MATN2, RPL30, 7 more genes
    nsv4614728copy number variation1nstd183human GRCh37 chr8: 99,169,690-99,199,971 , GRCh38.p12 chr8: 98,157,462-98,187,743 POP1, NIPAL2-AS1
    nsv4600479copy number variation1nstd183human GRCh37 chr8: 99,106,942-99,132,655 , GRCh38.p12 chr8: 98,094,714-98,120,427 POP1, RIDA
    nsv4525831copy number variation1nstd166human GRCh37.p13 chr8: 99,133,889-99,134,220 , GRCh38.p12 chr8: 98,121,661-98,121,992 POP1
    nsv4488604mobile element insertion1nstd166human GRCh37.p13 chr8: 99,137,171-99,137,171 , GRCh38.p12 chr8: 98,124,943-98,124,943 POP1
    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
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