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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076301inversion1nstd229human GRCh38 chr8: 66,503,152-66,503,854 , GRCh37.p13 chr8: 67,415,387-67,416,089 VXN
    nsv7070810inversion1nstd229human GRCh38 chr8: 66,491,972-66,496,662 , GRCh37.p13 chr8: 67,404,207-67,408,897 VXN
    nsv7064578inversion1nstd229human GRCh38 chr8: 66,496,511-66,500,180 , GRCh37.p13 chr8: 67,408,746-67,412,415 RNU6-1324P, VXN
    nsv6843253copy number variation1nstd229human GRCh38 chr8: 66,507,001-66,542,900 , GRCh37.p13 chr8: 67,419,236-67,455,135 VXN
    nsv6838672copy number variation1nstd229human GRCh38 chr8: 66,491,193-66,492,725 , GRCh37.p13 chr8: 67,403,428-67,404,960 VXN
    nsv6636205copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,261,729-68,676,568 , GRCh38.p12 chr8: 66,349,494-67,764,333 C8orf44-SGK3, SNHG6, 36 more genes
    nsv6575222inversion1nstd223human GRCh38 chr8: 66,503,152-66,503,854 , GRCh37.p13 chr8: 67,415,387-67,416,089 VXN
    nsv6421164copy number variation1nstd223human GRCh38 chr8: 66,497,848-66,502,543 , GRCh37.p13 chr8: 67,410,083-67,414,778 VXN, RNU6-1324P
    nsv6416618copy number variation1nstd223human GRCh38 chr8: 66,491,193-66,492,725 , GRCh37.p13 chr8: 67,403,428-67,404,960 VXN
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 LINC00967, LOC107986950, 64 more genes
    nsv6136691copy number variation1nstd213human GRCh37 chr8: 67,370,000-67,440,001 , GRCh38.p12 chr8: 66,457,765-66,527,766 ADHFE1, VXN, 2 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136068copy number variation1nstd213human GRCh37 chr8: 67,390,000-69,660,001 , GRCh38.p12 chr8: 66,477,765-68,747,766 ARFGEF1, SGK3, 41 more genes
    nsv5317589copy number variation1nstd204human GRCh38.p13 chr8: 66,411,276-66,741,302 , GRCh37.p13 chr8: 67,323,511-67,653,537 C8orf44, RRS1-DT, 11 more genes
    nsv5258948copy number variation1nstd204human GRCh38.p13 chr8: 66,411,201-66,741,300 , GRCh37.p13 chr8: 67,323,436-67,653,535 MYBL1, SGK3, 11 more genes
    nsv5105862mobile element insertion1nstd203human GRCh38 chr8: 66,498,387-66,498,394 , GRCh37.p13 chr8: 67,410,622-67,410,629 VXN
    nsv4965407copy number variation1nstd200human GRCh38 chr8: 66,491,193-66,492,726 , GRCh37.p13 chr8: 67,403,428-67,404,961 VXN
    nsv4965406copy number variation1nstd200human GRCh38 chr8: 66,411,286-66,741,296 , GRCh37.p13 chr8: 67,323,521-67,653,531 VCPIP1, RRS1-DT, 11 more genes
    nsv4960707copy number variation1nstd200human GRCh38 chr8: 66,497,848-66,502,543 , GRCh37.p13 chr8: 67,410,083-67,414,778 RNU6-1324P, VXN
    nsv4829065copy number variation1nstd200human GRCh37 chr8: 67,403,428-67,404,961 , GRCh38.p12 chr8: 66,491,193-66,492,726 VXN
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