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Items: 1 to 20 of 229

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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
    nsv7138885insertion1nstd232human GRCh37.p13 chr8: 125,551,529-125,551,529 , GRCh38.p12 chr8: 124,539,288-124,539,288 NDUFB9, TATDN1
    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
    nsv6856000copy number variation1nstd229human GRCh38 chr8: 124,373,188-128,390,224 , GRCh37.p13 chr8: 125,385,429-129,402,470 WASHC5, MIR4662B, 57 more genes
    nsv6854854copy number variation1nstd229human GRCh38 chr8: 124,417,443-124,594,587 , GRCh37.p13 chr8: 125,429,684-125,606,828 TRMT12, TATDN1, 6 more genes
    nsv6853419copy number variation1nstd229human GRCh38 chr8: 124,408,195-124,550,908 , GRCh37.p13 chr8: 125,420,436-125,563,149 TATDN1, MTSS1, 5 more genes
    nsv6846203copy number variation1nstd229human GRCh38 chr8: 124,544,187-124,548,184 , GRCh37.p13 chr8: 125,556,428-125,560,425 NDUFB9
    nsv6844101copy number variation1nstd229human GRCh38 chr8: 124,550,073-124,550,376 , GRCh37.p13 chr8: 125,562,314-125,562,617 MTSS1, NDUFB9
    nsv6843139copy number variation1nstd229human GRCh38 chr8: 124,544,801-124,549,400 , GRCh37.p13 chr8: 125,557,042-125,561,641 MTSS1, NDUFB9
    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
    nsv6632742copy number variation1nstd224human GRCh37 chr8: 125,268,800-125,716,371 , GRCh38.p12 chr8: 124,256,559-124,704,130 RNF139, RNU6-756P, 9 more genes
    nsv6558494inversion1nstd223human GRCh38 chr8: 124,541,127-124,541,607 , GRCh37.p13 chr8: 125,553,368-125,553,848 NDUFB9
    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
    nsv6294336mobile element insertion1nstd186human GRCh37 chr8: 125,557,051-125,557,102 , GRCh38.p12 chr8: 124,544,810-124,544,861 NDUFB9
    nsv6136313copy number variation1nstd213human GRCh37 chr8: 124,820,000-126,220,001 , GRCh38.p12 chr8: 123,807,760-125,207,759 NDUFB9, TRMT12, 28 more genes
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