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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142535copy number variation1nstd232human GRCh37.p13 chr7: 550,925-551,019 , GRCh38.p12 chr7: 511,288-511,382 PDGFA
    nsv7097362copy number variation1nstd102humanPathogenic GRCh37 chr7: 193,200-1,498,962 , GRCh38.p12 chr7: 193,200-1,459,326 ZFAND2A-DT, MICALL2, 28 more genes
    nsv7052768inversion1nstd229human GRCh38 chr7: 267,174-981,732 , GRCh37.p13 chr7: 307,140-1,021,368 PRKAR1B, FOXL3, 17 more genes
    nsv7050466inversion1nstd229human GRCh38 chr7: 226,743-953,102 , GRCh37.p13 chr7: 226,743-992,738 FAM20C, PRKAR1B-AS1, 15 more genes
    nsv6815553copy number variation1nstd229human GRCh38 chr7: 512,307-512,352 , GRCh37.p13 chr7: 551,944-551,989 PDGFA
    nsv6811902copy number variation1nstd229human GRCh38 chr7: 476,001-538,600 , GRCh37.p13 chr7: 515,638-578,237 PDGFA-DT, PDGFA
    nsv6808047copy number variation1nstd229human GRCh38 chr7: 252,604-498,921 , GRCh37.p13 chr7: 292,570-538,558 FOXL3-OT1, LOC112267991, 6 more genes
    nsv6807453copy number variation1nstd229human GRCh38 chr7: 473,702-561,406 , GRCh37.p13 chr7: 513,339-601,043 PRKAR1B-AS2, PDGFA, 2 more genes
    nsv6806647copy number variation1nstd229human GRCh38 chr7: 293,450-501,311 , GRCh37.p13 chr7: 333,416-540,948 LOC112267991, LOC116435278, 4 more genes
    nsv6803615copy number variation1nstd229human GRCh38 chr7: 490,526-496,457 , GRCh37.p13 chr7: 530,163-536,094 PDGFA
    nsv6803424copy number variation1nstd229human GRCh38 chr7: 506,694-506,978 , GRCh37.p13 chr7: 546,331-546,615 PDGFA
    nsv6802560copy number variation1nstd229human GRCh38 chr7: 398,101-667,200 , GRCh37.p13 chr7: 438,067-706,837 PRKAR1B-AS1, LOC105375119, 6 more genes
    nsv6802297copy number variation1nstd229human GRCh38 chr7: 505,321-505,652 , GRCh37.p13 chr7: 544,958-545,289 PDGFA
    nsv6636881copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,361-704,573 , GRCh38.p12 chr7: 43,361-664,936 LOC116435278, LOC105375115, 18 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632476copy number variation1nstd224human GRCh37 chr7: 93,811-2,255,893 , GRCh38.p12 chr7: 93,811-2,216,258 INTS1, DNAAF5, 52 more genes
    nsv6616549copy number variation1nstd223human GRCh38 chr7: 516,401-517,800 , GRCh37.p13 chr7: 556,038-557,437 PDGFA
    nsv6616169copy number variation1nstd223human GRCh38 chr7: 503,486-505,996 , GRCh37.p13 chr7: 543,123-545,633 PDGFA
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