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Items: 1 to 20 of 566

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066954inversion1nstd229human GRCh38 chr14: 30,982,854-31,221,335 , GRCh37.p13 chr14: 31,452,060-31,690,541 HECTD1, STRN3, 5 more genes
    nsv6957819copy number variation1nstd229human GRCh38 chr14: 29,967,815-31,229,292 , GRCh37.p13 chr14: 30,437,021-31,698,498 LOC100913082, RPS6P24, 19 more genes
    nsv6957025copy number variation1nstd229human GRCh38 chr14: 30,962,012-30,964,754 , GRCh37.p13 chr14: 31,431,218-31,433,960 HIGD1AP17, STRN3
    nsv6954313copy number variation1nstd229human GRCh38 chr14: 30,989,762-30,990,412 , GRCh37.p13 chr14: 31,458,968-31,459,618 STRN3
    nsv6953641copy number variation1nstd229human GRCh38 chr14: 30,930,561-30,933,102 , GRCh37.p13 chr14: 31,399,767-31,402,308 STRN3
    nsv6952996copy number variation1nstd229human GRCh38 chr14: 30,994,049-30,994,082 , GRCh37.p13 chr14: 31,463,255-31,463,288 STRN3
    nsv6952581copy number variation1nstd229human GRCh38 chr14: 30,989,345-30,997,440 , GRCh37.p13 chr14: 31,458,551-31,466,646 STRN3
    nsv6951305copy number variation1nstd229human GRCh38 chr14: 31,016,405-31,016,823 , GRCh37.p13 chr14: 31,485,611-31,486,029 STRN3, LOC100913082
    nsv6942837copy number variation1nstd229human GRCh38 chr14: 30,954,001-30,956,600 , GRCh37.p13 chr14: 31,423,207-31,425,806 STRN3
    nsv6942625copy number variation1nstd229human GRCh38 chr14: 30,982,343-30,982,716 , GRCh37.p13 chr14: 31,451,549-31,451,922 STRN3
    nsv6940438copy number variation1nstd229human GRCh38 chr14: 30,989,081-30,995,328 , GRCh37.p13 chr14: 31,458,287-31,464,534 STRN3
    nsv6939514copy number variation1nstd229human GRCh38 chr14: 30,934,059-30,934,222 , GRCh37.p13 chr14: 31,403,265-31,403,428 STRN3
    nsv6939198copy number variation1nstd229human GRCh38 chr14: 30,997,370-31,002,541 , GRCh37.p13 chr14: 31,466,576-31,471,747 STRN3
    nsv6637416copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,959,823-33,415,359 , GRCh38.p12 chr14: 24,490,617-32,946,153 SCFD1, RPL12P5, 94 more genes
    nsv6594918inversion1nstd223human GRCh38 chr14: 30,963,633-30,964,055 , GRCh37.p13 chr14: 31,432,839-31,433,261 STRN3, HIGD1AP17
    nsv6593177inversion1nstd223human GRCh38 chr14: 30,978,884-30,979,801 , GRCh37.p13 chr14: 31,448,090-31,449,007 STRN3
    nsv6591606inversion1nstd223human GRCh38 chr14: 30,656,873-33,818,146 , GRCh37.p13 chr14: 31,126,079-34,287,352 ARHGAP5-AS1, RN7SL660P, 37 more genes
    nsv6590982inversion1nstd223human GRCh38 chr14: 30,982,594-30,983,265 , GRCh37.p13 chr14: 31,451,800-31,452,471 STRN3
    nsv6585168inversion1nstd223human GRCh38 chr14: 30,944,734-30,945,399 , GRCh37.p13 chr14: 31,413,940-31,414,605 STRN3
    nsv6584608inversion1nstd223human GRCh38 chr14: 30,982,854-31,221,335 , GRCh37.p13 chr14: 31,452,060-31,690,541 AP4S1, HECTD1, 5 more genes
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