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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5486904copy number variation1nstd206human GRCh38 chr8: 109,541,203-109,541,329 , GRCh37.p13 chr8: 110,553,432-110,553,558 EBAG9
    nsv5379274translocation1nstd200human GRCh38 chr8: 109,577,392-109,577,392 , GRCh38 chr8: 109,564,492-109,564,492 , GRCh37.p13 chr8: 110,576,721-110,576,721 , GRCh37.p13 chr8: 110,589,621-110,589,621 SYBU, EBAG9
    nsv5335691translocation1nstd200human GRCh37 chr8: 110,589,621-110,589,621 , GRCh37 chr8: 110,576,721-110,576,721 , GRCh38.p12 chr8: 109,564,492-109,564,492 , GRCh38.p12 chr8: 109,577,392-109,577,392 EBAG9, SYBU
    nsv5319362copy number variation1nstd204human GRCh38.p13 chr8: 109,563,405-109,563,633 , GRCh37.p13 chr8: 110,575,634-110,575,862 EBAG9
    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
    nsv4965712copy number variation1nstd200human GRCh38 chr8: 109,482,094-109,564,343 , GRCh37.p13 chr8: 110,494,323-110,576,572 PKHD1L1, EBAG9
    nsv4961831copy number variation1nstd200human GRCh38 chr8: 109,553,561-109,557,869 , GRCh37.p13 chr8: 110,565,790-110,570,098 EBAG9
    nsv4822852copy number variation1nstd200human GRCh37 chr8: 110,565,790-110,570,098 , GRCh38.p12 chr8: 109,553,561-109,557,869 EBAG9
    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
    nsv4675496copy number variation1nstd102humanUncertain significance GRCh37 chr8: 109,858,221-110,567,774 , GRCh38.p12 chr8: 108,845,992-109,555,545 ENY2, LOC107984017, 7 more genes
    nsv4606170copy number variation1nstd183human GRCh37 chr8: 110,569,046-110,569,437 , GRCh38.p12 chr8: 109,556,817-109,557,208 EBAG9
    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
    nsv4167059copy number variation1nstd166human GRCh37.p13 chr8: 110,553,432-110,553,558 , GRCh38.p12 chr8: 109,541,203-109,541,329 EBAG9
    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
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