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Items: 1 to 20 of 291

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv7068103inversion1nstd229human GRCh38 chr17: 82,442,672-82,503,015 , GRCh37.p13 chr17: 80,400,548-80,460,891 HEXD, NARF, 3 more genes
    nsv6994498copy number variation1nstd229human GRCh38 chr17: 82,422,398-82,438,369 , GRCh37.p13 chr17: 80,380,274-80,396,245 HEXD
    nsv6993993copy number variation1nstd229human GRCh38 chr17: 82,433,201-82,462,600 , GRCh37.p13 chr17: 80,391,077-80,420,476 CYBC1, HEXD, 2 more genes
    nsv6988571copy number variation1nstd229human GRCh38 chr17: 82,428,520-82,437,441 , GRCh37.p13 chr17: 80,386,396-80,395,317 HEXD
    nsv6982690copy number variation1nstd229human GRCh38 chr17: 82,413,221-82,419,416 , GRCh37.p13 chr17: 80,371,097-80,377,292 OGFOD3, HEXD
    nsv6982221copy number variation1nstd229human GRCh38 chr17: 82,412,465-82,426,536 , GRCh37.p13 chr17: 80,370,341-80,384,412 HEXD, OGFOD3
    nsv6624531copy number variation1nstd224human GRCh37 chr17: 80,339,729-80,384,338 , GRCh38.p12 chr17: 82,381,853-82,426,462 HEXD, OGFOD3
    nsv6624530copy number variation1nstd224human GRCh37 chr17: 80,235,063-80,374,899 , GRCh38.p12 chr17: 82,277,187-82,417,023 CD7, UTS2R, 5 more genes
    nsv6624323copy number variation1nstd224human GRCh37 chr17: 80,274,603-80,464,614 , GRCh38.p12 chr17: 82,316,727-82,506,738 SECTM1, HEXD, 8 more genes
    nsv6624127copy number variation1nstd224human GRCh37 chr17: 80,280,865-80,464,614 , GRCh38.p12 chr17: 82,322,989-82,506,738 UTS2R, SECTM1, 7 more genes
    nsv6533522copy number variation1nstd223human GRCh38 chr17: 82,052,201-82,542,400 , GRCh37.p13 chr17: 80,010,077-80,500,276 MIR6787, CD7, 19 more genes
    nsv6533313copy number variation1nstd223human GRCh38 chr17: 82,294,456-82,671,315 , GRCh37.p13 chr17: 80,252,332-80,629,191 CD7, MIR4525, 14 more genes
    nsv6532965copy number variation1nstd223human GRCh38 chr17: 82,383,096-82,681,841 , GRCh37.p13 chr17: 80,340,972-80,639,717 OGFOD3, TRX-CAT1-8, 10 more genes
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 more genes
    nsv6521677copy number variation1nstd223human GRCh38 chr17: 82,422,874-82,423,451 , GRCh37.p13 chr17: 80,380,750-80,381,327 HEXD
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