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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7098159copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,545,411-125,559,374 , GRCh38.p12 chr8: 123,533,171-124,547,133 LOC105375738, LOC101927588, 20 more genes
    nsv7097891copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,515,613-126,379,127 , GRCh38.p12 chr8: 123,503,373-125,366,885 FER1L6-AS1, LOC112268031, 35 more genes
    nsv6854847copy number variation1nstd229human GRCh38 chr8: 123,638,368-123,909,763 , GRCh37.p13 chr8: 124,650,608-124,922,003 LOC105375739, ANXA13, 4 more genes
    nsv6852586copy number variation1nstd229human GRCh38 chr8: 123,709,963-123,711,337 , GRCh37.p13 chr8: 124,722,203-124,723,577 ANXA13
    nsv6850202copy number variation1nstd229human GRCh38 chr8: 123,711,675-123,715,379 , GRCh37.p13 chr8: 124,723,915-124,727,619 ANXA13
    nsv6849841copy number variation1nstd229human GRCh38 chr8: 123,720,801-123,724,900 , GRCh37.p13 chr8: 124,733,041-124,737,140 ANXA13, LOC105375739
    nsv6848888copy number variation1nstd229human GRCh38 chr8: 123,694,588-123,696,677 , GRCh37.p13 chr8: 124,706,828-124,708,917 ANXA13
    nsv6843279copy number variation1nstd229human GRCh38 chr8: 123,726,901-123,731,000 , GRCh37.p13 chr8: 124,739,141-124,743,240 LOC105375739, ANXA13
    nsv6842028copy number variation1nstd229human GRCh38 chr8: 123,691,835-123,692,023 , GRCh37.p13 chr8: 124,704,075-124,704,263 ANXA13
    nsv6840486copy number variation1nstd229human GRCh38 chr8: 123,686,866-123,686,972 , GRCh37.p13 chr8: 124,699,106-124,699,212 ANXA13
    nsv6839220copy number variation1nstd229human GRCh38 chr8: 123,710,623-123,710,807 , GRCh37.p13 chr8: 124,722,863-124,723,047 ANXA13
    nsv6839163copy number variation1nstd229human GRCh38 chr8: 123,674,370-123,680,020 , GRCh37.p13 chr8: 124,686,610-124,692,260 ANXA13
    nsv6838573copy number variation1nstd229human GRCh38 chr8: 123,702,891-123,716,062 , GRCh37.p13 chr8: 124,715,131-124,728,302 ANXA13
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632738copy number variation1nstd224human GRCh37 chr8: 124,658,193-124,907,620 , GRCh38.p12 chr8: 123,645,953-123,895,380 ANXA13, FAM91A1, 4 more genes
    nsv6430603copy number variation1nstd223human GRCh38 chr8: 123,708,366-123,709,804 , GRCh37.p13 chr8: 124,720,606-124,722,044 ANXA13
    nsv6429619copy number variation1nstd223human GRCh38 chr8: 123,713,887-123,716,234 , GRCh37.p13 chr8: 124,726,127-124,728,474 ANXA13
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