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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046818inversion1nstd229human GRCh38 chr5: 79,066,734-79,366,047 , GRCh37.p13 chr5: 78,362,557-78,661,870 BHMT, DMGDH, 6 more genes
    nsv7045990inversion1nstd229human GRCh38 chr5: 78,952,825-79,153,510 , GRCh37.p13 chr5: 78,248,648-78,449,333 DMGDH, LOC100505796, 3 more genes
    nsv7045119inversion1nstd229human GRCh38 chr5: 76,735,197-79,503,040 , GRCh37.p13 chr5: 76,031,022-78,798,863 RNU6ATAC36P, RPS3AP20, 39 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv7038776inversion1nstd229human GRCh38 chr5: 76,735,364-79,502,930 , GRCh37.p13 chr5: 76,031,189-78,798,753 HOMER1, LOC100505796, 39 more genes
    nsv6778008copy number variation1nstd229human GRCh38 chr5: 79,020,101-79,156,200 , GRCh37.p13 chr5: 78,315,924-78,452,023 BHMT2, BHMT, 1 more genes
    nsv6773744copy number variation1nstd229human GRCh38 chr5: 79,055,295-79,193,466 , GRCh37.p13 chr5: 78,351,118-78,489,289 BHMT2, DMGDH, 2 more genes
    nsv6769797copy number variation1nstd229human GRCh38 chr5: 79,055,744-79,066,208 , GRCh37.p13 chr5: 78,351,567-78,362,031 DMGDH
    nsv6768242copy number variation1nstd229human GRCh38 chr5: 79,053,519-79,053,573 , GRCh37.p13 chr5: 78,349,342-78,349,396 DMGDH
    nsv6767992copy number variation1nstd229human GRCh38 chr5: 79,004,225-79,015,914 , GRCh37.p13 chr5: 78,300,048-78,311,737 DMGDH
    nsv6763423copy number variation1nstd229human GRCh38 chr5: 77,899,127-80,222,849 , GRCh37.p13 chr5: 77,194,951-79,518,668 RNU6-183P, ARSB, 34 more genes
    nsv6762433copy number variation1nstd229human GRCh38 chr5: 79,056,873-79,064,077 , GRCh37.p13 chr5: 78,352,696-78,359,900 DMGDH
    nsv6762162copy number variation1nstd229human GRCh38 chr5: 78,796,013-79,169,970 , GRCh37.p13 chr5: 78,091,836-78,465,793 BHMT, DMGDH, 4 more genes
    nsv6636260copy number variation1nstd102humanUncertain significance GRCh37 chr5: 77,746,948-79,089,197 , GRCh38.p12 chr5: 78,451,125-79,793,374 RPL29P15, LOC102724530, 18 more genes
    nsv6574007inversion1nstd223human GRCh38 chr5: 78,998,927-78,999,283 , GRCh37.p13 chr5: 78,294,750-78,295,106 LOC100505796, DMGDH
    nsv6562879inversion1nstd223human GRCh38 chr5: 78,952,820-79,153,510 , GRCh37.p13 chr5: 78,248,643-78,449,333 ARSB, BHMT, 3 more genes
    nsv6408138copy number variation1nstd223human GRCh38 chr5: 79,061,978-79,064,377 , GRCh37.p13 chr5: 78,357,801-78,360,200 DMGDH
    nsv6404422copy number variation1nstd223human GRCh38 chr5: 79,037,464-79,039,475 , GRCh37.p13 chr5: 78,333,287-78,335,298 DMGDH
    nsv6403051copy number variation1nstd223human GRCh38 chr5: 79,066,001-79,072,200 , GRCh37.p13 chr5: 78,361,824-78,368,023 DMGDH, BHMT2
    nsv6402471copy number variation1nstd223human GRCh38 chr5: 79,069,301-79,069,900 , GRCh37.p13 chr5: 78,365,124-78,365,723 DMGDH, BHMT2
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