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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6748778copy number variation1nstd229human GRCh38 chr4: 69,775,074-70,688,486 , GRCh37.p13 chr4: 70,640,792-71,554,203 SULT1E1, SMR3A, 24 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
    nsv6746034copy number variation1nstd229human GRCh38 chr4: 70,584,944-70,713,558 , GRCh37.p13 chr4: 71,450,661-71,579,275 JCHAIN, RUFY3, 6 more genes
    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
    nsv6738560copy number variation1nstd229human GRCh38 chr4: 70,650,517-70,711,376 , GRCh37.p13 chr4: 71,516,234-71,577,093 LOC101927297, RUFY3, 4 more genes
    nsv6629979copy number variation1nstd224human GRCh37 chr4: 71,532,168-71,555,656 , GRCh38.p12 chr4: 70,666,451-70,689,939 LOC101927297, JCHAIN, 1 more genes
    nsv6567707inversion1nstd223human GRCh38 chr4: 70,659,353-70,660,488 , GRCh37.p13 chr4: 71,525,070-71,526,205 JCHAIN
    nsv6563301inversion1nstd223human GRCh38 chr4: 70,662,853-70,663,353 , GRCh37.p13 chr4: 71,528,570-71,529,070 JCHAIN
    nsv6560553inversion1nstd223human GRCh38 chr4: 70,662,694-70,663,288 , GRCh37.p13 chr4: 71,528,411-71,529,005 JCHAIN
    nsv6395465copy number variation1nstd223human GRCh38 chr4: 70,509,089-70,683,090 , GRCh37.p13 chr4: 71,374,806-71,548,807 ENAM, JCHAIN, 3 more genes
    nsv6383844copy number variation1nstd223human GRCh38 chr4: 70,584,944-70,713,558 , GRCh37.p13 chr4: 71,450,661-71,579,275 JCHAIN, LOC101927297, 6 more genes
    nsv6378457copy number variation1nstd223human GRCh38 chr4: 70,665,785-70,666,425 , GRCh37.p13 chr4: 71,531,502-71,532,142 JCHAIN
    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
    nsv6135356copy number variation1nstd213human GRCh37 chr4: 69,460,000-71,550,001 , GRCh38.p12 chr4: 68,594,282-70,684,284 CSN3, HTN3, 62 more genes
    nsv6134944copy number variation1nstd213human GRCh37 chr4: 71,330,000-72,380,001 , GRCh38.p12 chr4: 70,464,283-71,514,284 AMBN, DCK, 15 more genes
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
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