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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041217inversion1nstd229human GRCh38 chr5: 57,551,768-57,582,220 , GRCh37.p13 chr5: 56,847,595-56,878,047 LNCBRM
    nsv6776611copy number variation1nstd229human GRCh38 chr5: 57,612,739-57,620,036 , GRCh37.p13 chr5: 56,908,566-56,915,863 LNCBRM
    nsv6774631copy number variation1nstd229human GRCh38 chr5: 57,568,695-57,569,044 , GRCh37.p13 chr5: 56,864,522-56,864,871 LNCBRM
    nsv6773821copy number variation1nstd229human GRCh38 chr5: 57,574,708-57,574,823 , GRCh37.p13 chr5: 56,870,535-56,870,650 LNCBRM
    nsv6767040copy number variation1nstd229human GRCh38 chr5: 57,556,930-57,594,872 , GRCh37.p13 chr5: 56,852,757-56,890,699 LNCBRM
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6759306copy number variation1nstd229human GRCh38 chr5: 57,500,233-57,585,057 , GRCh37.p13 chr5: 56,796,060-56,880,884 LNCBRM, RMEL3
    nsv6758342copy number variation1nstd229human GRCh38 chr5: 57,597,701-57,601,000 , GRCh37.p13 chr5: 56,893,528-56,896,827 LNCBRM
    nsv6630356copy number variation1nstd224human GRCh37 chr5: 56,681,929-57,343,495 , GRCh38.p12 chr5: 57,386,102-58,047,668 ACTBL2, SALL4P1, 4 more genes
    nsv6413781copy number variation1nstd223human GRCh38 chr5: 57,571,746-57,572,103 , GRCh37.p13 chr5: 56,867,573-56,867,930 LNCBRM
    nsv6407524copy number variation1nstd223human GRCh38 chr5: 57,583,502-57,584,200 , GRCh37.p13 chr5: 56,879,329-56,880,027 LNCBRM
    nsv6402643copy number variation1nstd223human GRCh38 chr5: 57,464,513-57,594,318 , GRCh37.p13 chr5: 56,760,340-56,890,145 RMEL3, ACTBL2, 1 more genes
    nsv6399378copy number variation1nstd223human GRCh38 chr5: 57,500,233-57,585,054 , GRCh37.p13 chr5: 56,796,060-56,880,881 RMEL3, LNCBRM
    nsv6399365copy number variation1nstd223human GRCh38 chr5: 57,611,901-57,617,100 , GRCh37.p13 chr5: 56,907,728-56,912,927 LNCBRM
    nsv6260361mobile element insertion1nstd215human GRCh38 chr5: 57,590,571-57,590,571 , GRCh37.p13 chr5: 56,886,398-56,886,398 LNCBRM
    nsv6135669copy number variation1nstd213human GRCh37 chr5: 49,470,000-58,470,001 , GRCh38.p12 chr5: 50,174,166-59,174,175 , ASS1P9, 120 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv5902581copy number variation1nstd209human GRCh38 chr5: 57,595,239-57,595,308 , GRCh37.p13 chr5: 56,891,066-56,891,135 LNCBRM
    nsv5900903copy number variation1nstd209human GRCh38 chr5: 57,598,919-57,598,973 , GRCh37.p13 chr5: 56,894,746-56,894,800 LNCBRM
    nsv5728902mobile element insertion1nstd211human GRCh38 chr5: 57,617,460-57,617,460 , GRCh37.p13 chr5: 56,913,287-56,913,287 LNCBRM
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