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Items: 1 to 20 of 219

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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
    nsv7097417copy number variation1nstd102humanUncertain significance GRCh37 chr8: 118,811,951-120,844,804 , GRCh38.p12 chr8: 117,799,712-119,832,564 TAF2, SAMD12-AS1, 23 more genes
    nsv7097416copy number variation1nstd102humanPathogenic GRCh37 chr8: 117,859,739-120,844,804 , GRCh38.p12 chr8: 116,847,500-119,832,564 SAMD12, LOC105375717, 38 more genes
    nsv7097415copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,647,788-120,797,526 , GRCh38.p12 chr8: 116,635,549-119,785,286 LOC100286746, LOC105375717, 40 more genes
    nsv7077791inversion1nstd229human GRCh38 chr8: 117,677,720-119,359,389 , GRCh37.p13 chr8: 118,689,959-120,371,629 MIR548AZ, LOC105375725, 16 more genes
    nsv7072142inversion1nstd229human GRCh38 chr8: 113,332,988-120,659,210 , GRCh37.p13 chr8: 114,345,217-121,671,450 ENPP2, RAD21-AS1, 67 more genes
    nsv7058796inversion1nstd229human GRCh38 chr8: 117,263,675-119,216,537 , GRCh37.p13 chr8: 118,275,914-120,228,777 LOC100286746, SAMD12, 19 more genes
    nsv6849234copy number variation1nstd229human GRCh38 chr8: 118,823,513-119,091,800 , GRCh37.p13 chr8: 119,835,752-120,104,039 RNU6-12P, COLEC10, 4 more genes
    nsv6637672copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,645,068-121,684,174 , GRCh38.p12 chr8: 117,632,829-120,671,934 RPS26P35, LOC105375723, 34 more genes
    nsv6637485copy number variation1nstd102humanUncertain significance GRCh37 chr8: 118,492,577-121,075,880 , GRCh38.p12 chr8: 117,480,338-120,063,641 LOC100286746, DEPTOR, 32 more genes
    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
    nsv6432437copy number variation1nstd223human GRCh38 chr8: 117,474,988-120,065,962 , GRCh37.p13 chr8: 118,487,227-121,078,201 RPS26P35, LOC105375723, 32 more genes
    nsv6427691copy number variation1nstd223human GRCh38 chr8: 118,823,513-119,091,800 , GRCh37.p13 chr8: 119,835,752-120,104,039 COLEC10, LOC100286746, 4 more genes
    nsv6423802copy number variation1nstd223human GRCh38 chr8: 119,063,134-119,063,576 , GRCh37.p13 chr8: 120,075,373-120,075,815 COLEC10, LOC101927513
    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
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
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