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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7072131inversion1nstd229human GRCh38 chr20: 53,548,074-57,294,874 , GRCh37.p13 chr20: 52,164,613-55,869,930 CBLN4, RNU6-1146P, 46 more genes
    nsv7071269inversion1nstd229human GRCh38 chr20: 51,579,374-58,024,568 , GRCh37.p13 chr20: 50,195,913-56,599,624 CBLN4, LOC105372693, 89 more genes
    nsv7063616inversion1nstd229human GRCh38 chr20: 51,911,434-57,961,609 , GRCh37.p13 chr20: 50,527,973-56,536,665 FAM210B, BCAS1, 81 more genes
    nsv7058989inversion1nstd229human GRCh38 chr20: 52,927,440-57,459,107 , GRCh37.p13 chr20: 51,543,979-56,034,163 FAM210B, RPS4XP3, 61 more genes
    nsv7058267inversion1nstd229human GRCh38 chr20: 51,559,821-57,992,303 , GRCh37.p13 chr20: 50,176,360-56,567,359 LOC105372683, MRPS33P4, 89 more genes
    nsv7058201inversion1nstd229human GRCh38 chr20: 51,845,371-57,066,404 , GRCh37.p13 chr20: 50,461,910-55,641,460 RNU6-347P, RPS4XP3, 61 more genes
    nsv7037859copy number variation1nstd229human GRCh38 chr20: 56,519,650-56,522,001 , GRCh37.p13 chr20: 55,094,706-55,097,057 GCNT7, RTF2
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7036177copy number variation1nstd229human GRCh38 chr20: 54,492,617-57,541,251 , GRCh37.p13 chr20: 53,109,156-56,116,307 SPO11, BMP7, 47 more genes
    nsv7030777copy number variation1nstd229human GRCh38 chr20: 56,492,448-56,496,368 , GRCh37.p13 chr20: 55,067,504-55,071,424 RTF2, GCNT7
    nsv7027878copy number variation1nstd229human GRCh38 chr20: 56,252,646-56,527,506 , GRCh37.p13 chr20: 54,827,702-55,102,562 FAM209A, RPL39P, 7 more genes
    nsv7026030copy number variation1nstd229human GRCh38 chr20: 56,510,412-56,522,105 , GRCh37.p13 chr20: 55,085,468-55,097,161 RTF2, GCNT7
    nsv7024719copy number variation1nstd229human GRCh38 chr20: 56,505,607-56,526,510 , GRCh37.p13 chr20: 55,080,663-55,101,566 RTF2, GCNT7, 2 more genes
    nsv7021126copy number variation1nstd229human GRCh38 chr20: 55,610,437-57,355,505 , GRCh37.p13 chr20: 54,220,678-55,930,561 SPO11, LOC105376989, 35 more genes
    nsv6637604copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,517,925-55,402,822 , GRCh38.p12 chr20: 53,901,386-56,827,766 DOK5, LOC107984001, 34 more genes
    nsv6626590copy number variation1nstd224human GRCh37 chr20: 55,101,065-55,116,737 , GRCh38.p12 chr20: 56,526,009-56,541,681 GCNT7, FAM209A, 1 more genes
    nsv6626582copy number variation1nstd224human GRCh37 chr20: 55,101,065-55,111,364 , GRCh38.p12 chr20: 56,526,009-56,536,308 GCNT7, FAM209A, 1 more genes
    nsv6554850copy number variation1nstd223human GRCh38 chr20: 56,510,774-56,538,563 , GRCh37.p13 chr20: 55,085,830-55,113,619 RTF2, GCNT7, 2 more genes
    nsv6551796copy number variation1nstd223human GRCh38 chr20: 56,526,316-56,536,648 , GRCh37.p13 chr20: 55,101,372-55,111,704 FAM209A, GCNT7, 1 more genes
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