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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141116copy number variation1nstd232human GRCh37.p13 chr17: 80,674,389-80,674,468 , GRCh38.p12 chr17: 82,716,513-82,716,592 FN3KRP, LOC101929552
    nsv7137148copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,656,331-81,009,672 , GRCh38.p12 chr17: 82,698,455-83,051,796 ZNF750, FN3KRP, 5 more genes
    nsv7098933copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,004,063-83,087,346 , GRCh37.p13 chr17: 79,961,939-81,045,222 ZNF750, LINC01970, 37 more genes
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095424copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,332,201-80,758,892 , GRCh38.p12 chr17: 82,374,325-82,801,016 CYBC1, TRX-CAT1-8, 15 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7067498inversion1nstd229human GRCh38 chr17: 82,700,440-82,715,184 , GRCh37.p13 chr17: 80,658,316-80,673,060 FN3KRP, LOC101929552
    nsv7063392inversion1nstd229human GRCh38 chr17: 82,609,707-82,780,313 , GRCh37.p13 chr17: 80,567,583-80,738,189 RAB40B, FN3KRP, 5 more genes
    nsv6995894copy number variation1nstd229human GRCh38 chr17: 82,528,831-82,827,183 , GRCh37.p13 chr17: 80,486,707-80,785,059 LOC105371942, FN3KRP, 8 more genes
    nsv6995527copy number variation1nstd229human GRCh38 chr17: 82,681,594-82,916,948 , GRCh37.p13 chr17: 80,639,470-80,874,824 LOC101929552, TBCD, 4 more genes
    nsv6990525copy number variation1nstd229human GRCh38 chr17: 82,708,698-82,716,353 , GRCh37.p13 chr17: 80,666,574-80,674,229 FN3KRP, LOC101929552
    nsv6985899copy number variation1nstd229human GRCh38 chr17: 82,709,064-82,956,275 , GRCh37.p13 chr17: 80,666,940-80,914,151 FN3K, TBCD, 4 more genes
    nsv6985281copy number variation1nstd229human GRCh38 chr17: 82,654,201-82,957,097 , GRCh37.p13 chr17: 80,612,077-80,914,973 B3GNTL1, MIR4525, 6 more genes
    nsv6983693copy number variation1nstd229human GRCh38 chr17: 82,697,149-82,736,865 , GRCh37.p13 chr17: 80,655,025-80,694,741 RAB40B, FN3K, 2 more genes
    nsv6637647copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,585,033-81,041,938 , GRCh38.p12 chr17: 82,627,157-83,084,062 ZNF750, FN3KRP, 8 more genes
    nsv6634437copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 80,496,771-81,195,210 , GRCh38.p12 chr17: 82,538,895-83,247,441 FOXK2, TBCD, 16 more genes
    nsv6532503copy number variation1nstd223human GRCh38 chr17: 82,709,064-82,956,275 , GRCh37.p13 chr17: 80,666,940-80,914,151 FN3KRP, B3GNTL1, 4 more genes
    nsv6529829copy number variation1nstd223human GRCh38 chr17: 82,664,860-83,182,172 , GRCh37.p13 chr17: 80,622,736-81,129,941 LOC101929552, TBCD, 9 more genes
    nsv6522025copy number variation1nstd223human GRCh38 chr17: 82,685,213-82,796,284 , GRCh37.p13 chr17: 80,643,089-80,754,160 FN3KRP, LOC101929552, 3 more genes
    nsv6517928copy number variation1nstd223human GRCh38 chr17: 82,706,946-82,739,809 , GRCh37.p13 chr17: 80,664,822-80,697,685 FN3K, FN3KRP, 1 more genes
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