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Items: 1 to 20 of 232

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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
    nsv7077052inversion1nstd229human GRCh38 chr8: 122,556,885-123,611,669 , GRCh37.p13 chr8: 123,569,124-124,623,909 RNY4P5, ZHX2, 27 more genes
    nsv7074985inversion1nstd229human GRCh38 chr8: 123,013,866-123,013,917 , GRCh37.p13 chr8: 124,026,106-124,026,157 DERL1
    nsv7064991inversion1nstd229human GRCh38 chr8: 122,266,535-123,404,204 , GRCh37.p13 chr8: 123,278,774-124,416,444 FAM83A, LOC107986904, 26 more genes
    nsv6853853copy number variation1nstd229human GRCh38 chr8: 123,024,283-123,024,463 , GRCh37.p13 chr8: 124,036,523-124,036,703 DERL1
    nsv6846220copy number variation1nstd229human GRCh38 chr8: 123,016,721-123,020,706 , GRCh37.p13 chr8: 124,028,961-124,032,946 DERL1
    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
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6136310copy number variation1nstd213human GRCh37 chr8: 123,620,000-124,800,001 , GRCh38.p12 chr8: 122,607,761-123,787,761 TBC1D31, FAM91A1, 31 more genes
    nsv6136309copy number variation1nstd213human GRCh37 chr8: 122,920,000-127,650,001 , GRCh38.p12 chr8: 121,907,761-126,637,756 TBC1D31, FAM91A1, 77 more genes
    nsv6136239copy number variation1nstd213human GRCh37 chr8: 123,850,000-124,200,001 , GRCh38.p12 chr8: 122,837,761-123,187,761 ZHX2, DERL1, 5 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6135818copy number variation1nstd213human GRCh37 chr8: 121,840,000-124,320,001 , GRCh38.p12 chr8: 120,827,760-123,307,761 DERL1, CDK5P1, 27 more genes
    nsv5379382translocation1nstd200human GRCh38 chr8: 123,040,155-123,040,155 , GRCh38 chr8: 123,040,215-123,040,215 , GRCh37.p13 chr8: 124,052,455-124,052,455 , GRCh37.p13 chr8: 124,052,395-124,052,395 DERL1, TBC1D31
    nsv5060033copy number variation1nstd102humanUncertain significance GRCh37 chr8: 121,938,227-125,485,728 , GRCh38.p12 chr8: 120,925,987-124,473,487 RNU6-756P, FAM83A, 53 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
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