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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
    nsv6855756copy number variation1nstd229human GRCh38 chr8: 124,474,691-124,490,427 , GRCh37.p13 chr8: 125,486,932-125,502,668 TATDN1, RNF139, 1 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
    nsv6848506copy number variation1nstd229human GRCh38 chr8: 124,482,946-124,491,507 , GRCh37.p13 chr8: 125,495,187-125,503,748 TATDN1, RNF139
    nsv6843839copy number variation1nstd229human GRCh38 chr8: 124,494,555-124,494,732 , GRCh37.p13 chr8: 125,506,796-125,506,973 TATDN1
    nsv6842797copy number variation1nstd229human GRCh38 chr8: 124,512,987-124,523,699 , GRCh37.p13 chr8: 125,525,228-125,535,940 TATDN1
    nsv6841106copy number variation1nstd229human GRCh38 chr8: 124,472,309-124,492,204 , GRCh37.p13 chr8: 125,484,550-125,504,445 RNF139-DT, RNF139, 1 more genes
    nsv6838240copy number variation1nstd229human GRCh38 chr8: 124,489,759-124,502,389 , GRCh37.p13 chr8: 125,502,000-125,514,630 TATDN1
    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
    nsv6632248copy number variation1nstd224human GRCh37 chr8: 125,498,341-125,520,892 , GRCh38.p12 chr8: 124,486,100-124,508,651 RNF139, TATDN1, 1 more genes
    nsv6569994inversion1nstd223human GRCh38 chr8: 124,490,441-124,490,931 , GRCh37.p13 chr8: 125,502,682-125,503,172 TATDN1
    nsv6568757inversion1nstd223human GRCh38 chr8: 124,504,770-124,505,263 , GRCh37.p13 chr8: 125,517,011-125,517,504 TATDN1
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