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Items: 1 to 20 of 451

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055641inversion1nstd229human GRCh38 chr5: 79,236,588-79,236,688 , GRCh37.p13 chr5: 78,532,411-78,532,511 JMY
    nsv7050546inversion1nstd229human GRCh38 chr5: 79,227,383-80,480,748 , GRCh37.p13 chr5: 78,523,206-79,776,567 TENT2, SPZ1, 27 more genes
    nsv7046818inversion1nstd229human GRCh38 chr5: 79,066,734-79,366,047 , GRCh37.p13 chr5: 78,362,557-78,661,870 BHMT, DMGDH, 6 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
    nsv7044314inversion1nstd229human GRCh38 chr5: 79,279,799-79,333,190 , GRCh37.p13 chr5: 78,575,622-78,629,013 LOC102724530, RPS3AP20, 1 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
    nsv7040471inversion1nstd229human GRCh38 chr5: 79,267,908-79,479,752 , GRCh37.p13 chr5: 78,563,731-78,775,575 HOMER1, RPS3AP20, 4 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
    nsv6777667copy number variation1nstd229human GRCh38 chr5: 79,293,557-79,298,533 , GRCh37.p13 chr5: 78,589,380-78,594,356 JMY
    nsv6776822copy number variation1nstd229human GRCh38 chr5: 79,243,301-79,283,300 , GRCh37.p13 chr5: 78,539,124-78,579,123 RPS3AP20, JMY
    nsv6775582copy number variation1nstd229human GRCh38 chr5: 79,081,601-79,283,300 , GRCh37.p13 chr5: 78,377,424-78,579,123 BHMT, RPS3AP20, 3 more genes
    nsv6775147copy number variation1nstd229human GRCh38 chr5: 79,120,982-79,479,817 , GRCh37.p13 chr5: 78,416,805-78,775,640 RNY3P1, LOC107986426, 6 more genes
    nsv6773670copy number variation1nstd229human GRCh38 chr5: 79,272,652-79,276,929 , GRCh37.p13 chr5: 78,568,475-78,572,752 JMY
    nsv6770284copy number variation1nstd229human GRCh38 chr5: 79,309,756-79,348,688 , GRCh37.p13 chr5: 78,605,579-78,644,511 JMY, LOC102724530, 1 more genes
    nsv6767334copy number variation1nstd229human GRCh38 chr5: 79,242,391-79,262,439 , GRCh37.p13 chr5: 78,538,214-78,558,262 JMY
    nsv6763975copy number variation1nstd229human GRCh38 chr5: 79,243,387-79,257,759 , GRCh37.p13 chr5: 78,539,210-78,553,582 JMY
    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
    nsv6763261copy number variation1nstd229human GRCh38 chr5: 79,244,881-79,631,540 , GRCh37.p13 chr5: 78,540,704-78,927,363 JMY, HOMER1, 8 more genes
    nsv6761882copy number variation1nstd229human GRCh38 chr5: 79,254,201-79,258,000 , GRCh37.p13 chr5: 78,550,024-78,553,823 JMY
    nsv6761607copy number variation1nstd229human GRCh38 chr5: 79,265,049-79,269,990 , GRCh37.p13 chr5: 78,560,872-78,565,813 JMY
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