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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140699insertion1nstd232human GRCh37.p13 chr4: 71,691,147-71,691,147 , GRCh38.p12 chr4: 70,825,430-70,825,430 GRSF1
    nsv7057201inversion1nstd229human GRCh38 chr4: 70,218,974-71,891,696 , GRCh37.p13 chr4: 71,084,691-72,757,413 SMR3A, CSN3, 25 more genes
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6742566copy number variation1nstd229human GRCh38 chr4: 70,841,526-70,848,289 , GRCh37.p13 chr4: 71,707,243-71,714,006 GRSF1
    nsv6738720copy number variation1nstd229human GRCh38 chr4: 70,598,088-71,269,981 , GRCh37.p13 chr4: 71,463,805-72,135,698 SLC4A4, GRSF1, 11 more genes
    nsv6738491copy number variation1nstd229human GRCh38 chr4: 70,821,101-70,834,900 , GRCh37.p13 chr4: 71,686,818-71,700,617 GRSF1
    nsv6636207copy number variation1nstd102humanUncertain significance GRCh37 chr4: 71,643,631-71,975,779 , GRCh38.p12 chr4: 70,777,914-71,110,062 DCK, RNU6-891P, 4 more genes
    nsv6574291inversion1nstd223human GRCh38 chr4: 70,827,288-70,828,741 , GRCh37.p13 chr4: 71,693,005-71,694,458 GRSF1
    nsv6564691inversion1nstd223human GRCh38 chr4: 70,823,663-70,824,410 , GRCh37.p13 chr4: 71,689,380-71,690,127 GRSF1
    nsv6564619inversion1nstd223human GRCh38 chr4: 70,834,092-70,834,660 , GRCh37.p13 chr4: 71,699,809-71,700,377 GRSF1
    nsv6561061inversion1nstd223human GRCh38 chr4: 70,823,820-70,824,199 , GRCh37.p13 chr4: 71,689,537-71,689,916 GRSF1
    nsv6388438copy number variation1nstd223human GRCh38 chr4: 70,830,587-70,831,087 , GRCh37.p13 chr4: 71,696,304-71,696,804 GRSF1
    nsv6381077copy number variation1nstd223human GRCh38 chr4: 70,714,621-70,822,630 , GRCh37.p13 chr4: 71,580,338-71,688,347 GRSF1, RUFY3
    nsv6379266copy number variation1nstd223human GRCh38 chr4: 70,834,097-70,843,912 , GRCh37.p13 chr4: 71,699,814-71,709,629 GRSF1
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6290740copy number variation1nstd102humanUncertain significance GRCh37 chr4: 71,561,781-72,059,983 , GRCh38.p12 chr4: 70,696,064-71,194,266 RNU6-520P, RNU6-784P, 6 more genes
    nsv6155402copy number variation1nstd214human GRCh38 chr4: 70,840,052-70,840,154 , GRCh37.p13 chr4: 71,705,769-71,705,871 GRSF1
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