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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7095425copy number variation1nstd102humanPathogenic GRCh37 chr17: 80,710,070-80,901,020 , GRCh38.p12 chr17: 82,752,194-82,943,144 B3GNTL1, TBCD, 1 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
    nsv7076894inversion1nstd229human GRCh38 chr17: 82,792,114-82,983,211 , GRCh37.p13 chr17: 80,749,990-80,941,087 B3GNTL1, TBCD, 1 more genes
    nsv7070422inversion1nstd229human GRCh38 chr17: 82,824,238-82,975,531 , GRCh37.p13 chr17: 80,782,114-80,933,407 B3GNTL1, TBCD, 1 more genes
    nsv7066353inversion1nstd229human GRCh38 chr17: 82,834,185-83,204,915 , GRCh37.p13 chr17: 80,792,061-81,152,684 LOC105371948, LOC101929650, 5 more genes
    nsv6995670copy number variation1nstd229human GRCh38 chr17: 82,804,019-82,828,161 , GRCh37.p13 chr17: 80,761,895-80,786,037 TBCD, ZNF750
    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
    nsv6994100copy number variation1nstd229human GRCh38 chr17: 82,741,786-82,914,800 , GRCh37.p13 chr17: 80,699,662-80,872,676 TBCD, FN3K, 1 more genes
    nsv6992994copy number variation1nstd229human GRCh38 chr17: 82,788,987-83,087,357 , GRCh37.p13 chr17: 80,746,863-81,045,233 B3GNTL1, METRNL, 2 more genes
    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
    nsv6985726copy number variation1nstd229human GRCh38 chr17: 82,832,636-82,839,926 , GRCh37.p13 chr17: 80,790,512-80,797,802 TBCD, ZNF750
    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
    nsv6985191copy number variation1nstd229human GRCh38 chr17: 82,741,951-82,897,888 , GRCh37.p13 chr17: 80,699,827-80,855,764 TBCD, ZNF750, 1 more genes
    nsv6982990copy number variation1nstd229human GRCh38 chr17: 82,834,301-82,840,300 , GRCh37.p13 chr17: 80,792,177-80,798,176 TBCD, ZNF750
    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
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