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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
    nsv7139640copy number variation1nstd232human GRCh37.p13 chr8: 130,659,482-130,659,531 , GRCh38.p12 chr8: 129,647,236-129,647,285 CCDC26
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7066356inversion1nstd229human GRCh38 chr8: 129,677,742-129,696,497 , GRCh37.p13 chr8: 130,689,988-130,708,743 CCDC26
    nsv7066203inversion1nstd229human GRCh38 chr8: 129,405,246-129,405,285 , GRCh37.p13 chr8: 130,417,492-130,417,531 CCDC26
    nsv7065044inversion1nstd229human GRCh38 chr8: 129,328,678-129,365,039 , GRCh37.p13 chr8: 130,340,924-130,377,285 CCDC26
    nsv7062540inversion1nstd229human GRCh38 chr8: 126,857,766-129,574,185 , GRCh37.p13 chr8: 127,870,011-130,586,431 CASC21, POU5F1B, 28 more genes
    nsv6857577copy number variation1nstd229human GRCh38 chr8: 129,451,667-129,462,929 , GRCh37.p13 chr8: 130,463,913-130,475,175 CCDC26
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6856912copy number variation1nstd229human GRCh38 chr8: 129,620,087-129,629,521 , GRCh37.p13 chr8: 130,632,333-130,641,767 CCDC26
    nsv6854669copy number variation1nstd229human GRCh38 chr8: 129,403,801-129,426,900 , GRCh37.p13 chr8: 130,416,047-130,439,146 CCDC26
    nsv6854534copy number variation1nstd229human GRCh38 chr8: 129,483,531-129,489,999 , GRCh37.p13 chr8: 130,495,777-130,502,245 MIR3686, CCDC26
    nsv6853011copy number variation1nstd229human GRCh38 chr8: 129,421,101-129,430,600 , GRCh37.p13 chr8: 130,433,347-130,442,846 CCDC26
    nsv6852376copy number variation1nstd229human GRCh38 chr8: 129,436,060-129,491,355 , GRCh37.p13 chr8: 130,448,306-130,503,601 CCDC26, MIR3686
    nsv6852346copy number variation1nstd229human GRCh38 chr8: 129,403,201-129,424,400 , GRCh37.p13 chr8: 130,415,447-130,436,646 CCDC26
    nsv6851935copy number variation1nstd229human GRCh38 chr8: 129,403,301-129,425,900 , GRCh37.p13 chr8: 130,415,547-130,438,146 CCDC26
    nsv6851413copy number variation1nstd229human GRCh38 chr8: 129,389,396-129,389,925 , GRCh37.p13 chr8: 130,401,642-130,402,171 CCDC26
    nsv6850788copy number variation1nstd229human GRCh38 chr8: 129,368,953-129,379,274 , GRCh37.p13 chr8: 130,381,199-130,391,520 CCDC26
    nsv6850586copy number variation1nstd229human GRCh38 chr8: 129,595,324-129,595,451 , GRCh37.p13 chr8: 130,607,570-130,607,697 CCDC26
    nsv6850576copy number variation1nstd229human GRCh38 chr8: 129,357,801-129,418,000 , GRCh37.p13 chr8: 130,370,047-130,430,246 CCDC26
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