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Items: 1 to 20 of 221

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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
    nsv7094997copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,891,090-80,333,370 , GRCh38.p12 chr17: 81,933,214-82,375,494 LOC105371939, LINC01970, 22 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6982969copy number variation1nstd229human GRCh38 chr17: 82,321,046-82,386,846 , GRCh37.p13 chr17: 80,278,922-80,344,722 TEX19, UTS2R, 2 more genes
    nsv6980162copy number variation1nstd229human GRCh38 chr17: 82,276,139-82,416,061 , GRCh37.p13 chr17: 80,234,015-80,373,937 CD7, OGFOD3, 4 more genes
    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
    nsv6526179copy number variation1nstd223human GRCh38 chr17: 82,276,071-82,416,094 , GRCh37.p13 chr17: 80,233,947-80,373,970 OGFOD3, SECTM1, 4 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
    nsv6518969copy number variation1nstd223human GRCh38 chr17: 82,181,801-82,461,700 , GRCh37.p13 chr17: 80,139,677-80,419,576 LINC01970, NARF, 12 more genes
    nsv6517992copy number variation1nstd223human GRCh38 chr17: 82,266,795-82,432,903 , GRCh37.p13 chr17: 80,224,671-80,390,779 CSNK1D, SECTM1, 6 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6314037copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,976,464-81,041,938 , GRCh38.p12 chr17: 82,018,588-83,084,062 OGFOD3, DCXR-DT, 36 more genes
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
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