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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145302copy number variation1nstd232human GRCh37.p13 chr7: 933,450-933,532 , GRCh38.p12 chr7: 893,813-893,895 GET4
    nsv7141299insertion1nstd232human GRCh37.p13 chr7: 930,705-930,705 , GRCh38.p12 chr7: 891,068-891,068 GET4
    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
    nsv7049824inversion1nstd229human GRCh38 chr7: 547,787-928,437 , GRCh37.p13 chr7: 587,424-968,073 ADAP1, PRKAR1B, 6 more genes
    nsv7048812inversion1nstd229human GRCh38 chr7: 732,942-1,080,874 , GRCh37.p13 chr7: 772,579-1,120,510 GPR146, LOC105375120, 8 more genes
    nsv6817310copy number variation1nstd229human GRCh38 chr7: 877,829-881,352 , GRCh37.p13 chr7: 917,466-920,989 GET4
    nsv6817286copy number variation1nstd229human GRCh38 chr7: 876,323-881,908 , GRCh37.p13 chr7: 915,960-921,545 GET4
    nsv6813333copy number variation1nstd229human GRCh38 chr7: 875,428-875,457 , GRCh37.p13 chr7: 915,065-915,094 GET4, SUN1
    nsv6805429copy number variation1nstd229human GRCh38 chr7: 876,314-876,464 , GRCh37.p13 chr7: 915,951-916,101 GET4
    nsv6802309copy number variation1nstd229human GRCh38 chr7: 886,676-886,714 , GRCh37.p13 chr7: 926,313-926,351 GET4
    nsv6800698copy number variation1nstd229human GRCh38 chr7: 890,101-1,018,300 , GRCh37.p13 chr7: 929,738-1,057,936 CYP2W1, GET4, 3 more genes
    nsv6798922copy number variation1nstd229human GRCh38 chr7: 680,698-1,325,106 , GRCh37.p13 chr7: 720,335-1,364,742 DNAAF5, MIR339, 14 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
    nsv6617836copy number variation1nstd223human GRCh38 chr7: 877,829-881,347 , GRCh37.p13 chr7: 917,466-920,984 GET4
    nsv6606009copy number variation1nstd223human GRCh38 chr7: 602,600-905,284 , GRCh37.p13 chr7: 642,237-944,921 PRKAR1B, GET4, 5 more genes
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