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Items: 1 to 20 of 313

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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
    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
    nsv7064374inversion1nstd229human GRCh38 chr17: 82,046,151-82,149,895 , GRCh37.p13 chr17: 80,004,027-80,107,771 GPS1, CCDC57, 4 more genes
    nsv7061699inversion1nstd229human GRCh38 chr17: 81,983,159-82,059,180 , GRCh37.p13 chr17: 79,941,035-80,017,056 RAC3, CENPX, 7 more genes
    nsv6997997copy number variation1nstd229human GRCh38 chr17: 81,965,405-82,127,093 , GRCh37.p13 chr17: 79,923,281-80,084,969 ASPSCR1, CCDC57, 11 more genes
    nsv6989489copy number variation1nstd229human GRCh38 chr17: 81,929,777-82,073,240 , GRCh37.p13 chr17: 79,887,653-80,031,116 PYCR1, ASPSCR1, 12 more genes
    nsv6984488copy number variation1nstd229human GRCh38 chr17: 82,036,901-82,098,400 , GRCh37.p13 chr17: 79,994,777-80,056,276 SNORD134, GPS1, 5 more genes
    nsv6983060copy number variation1nstd229human GRCh38 chr17: 82,048,825-82,048,918 , GRCh37.p13 chr17: 80,006,701-80,006,794 RFNG
    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
    nsv6530652copy number variation1nstd223human GRCh38 chr17: 81,965,405-82,127,093 , GRCh37.p13 chr17: 79,923,281-80,084,969 RAC3, FASN, 11 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
    nsv6519994copy number variation1nstd223human GRCh38 chr17: 82,016,200-82,049,645 , GRCh37.p13 chr17: 79,974,076-80,007,521 RAC3, CENPX, 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
    nsv6288965insertion1nstd214human GRCh38 chr17: 82,048,907-82,048,907 , GRCh37.p13 chr17: 80,006,783-80,006,783 RFNG
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6131211insertion1nstd186human GRCh37 chr17: 80,006,851-80,006,898 , GRCh38.p12 chr17: 82,048,975-82,049,022 RFNG
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