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Items: 1 to 20 of 469

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096788copy number variation1nstd102humanPathogenic GRCh37 chr5: 76,115,008-78,281,071 , GRCh38.p12 chr5: 76,819,183-78,985,248 LHFPL2, OTP, 27 more genes
    nsv7050643inversion1nstd229human GRCh38 chr5: 77,339,476-78,646,078 , GRCh37.p13 chr5: 76,635,301-77,941,901 LHFPL2, RNU6-183P, 15 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
    nsv6775648copy number variation1nstd229human GRCh38 chr5: 78,431,001-78,473,900 , GRCh37.p13 chr5: 77,726,825-77,769,723 SCAMP1
    nsv6774988copy number variation1nstd229human GRCh38 chr5: 78,404,513-78,406,676 , GRCh37.p13 chr5: 77,700,337-77,702,500 SCAMP1
    nsv6773049copy number variation1nstd229human GRCh38 chr5: 78,465,183-78,468,159 , GRCh37.p13 chr5: 77,761,006-77,763,982 SCAMP1
    nsv6770767copy number variation1nstd229human GRCh38 chr5: 78,376,701-78,429,800 , GRCh37.p13 chr5: 77,672,525-77,725,624 SCAMP1
    nsv6768809copy number variation1nstd229human GRCh38 chr5: 78,417,245-78,417,368 , GRCh37.p13 chr5: 77,713,069-77,713,192 SCAMP1
    nsv6765259copy number variation1nstd229human GRCh38 chr5: 78,427,216-78,438,328 , GRCh37.p13 chr5: 77,723,040-77,734,152 SCAMP1
    nsv6763909copy number variation1nstd229human GRCh38 chr5: 78,435,401-78,462,600 , GRCh37.p13 chr5: 77,731,225-77,758,423 SCAMP1
    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
    nsv6761941copy number variation1nstd229human GRCh38 chr5: 78,420,427-78,420,565 , GRCh37.p13 chr5: 77,716,251-77,716,389 SCAMP1
    nsv6758617copy number variation1nstd229human GRCh38 chr5: 78,406,849-78,449,298 , GRCh37.p13 chr5: 77,702,673-77,745,122 SCAMP1
    nsv6758481copy number variation1nstd229human GRCh38 chr5: 78,471,747-78,474,749 , GRCh37.p13 chr5: 77,767,570-77,770,572 SCAMP1
    nsv6758384copy number variation1nstd229human GRCh38 chr5: 78,446,714-78,525,723 , GRCh37.p13 chr5: 77,742,538-77,821,546 LHFPL2, SCAMP1
    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
    nsv6630882copy number variation1nstd224human GRCh37 chr5: 77,606,215-77,816,427 , GRCh38.p12 chr5: 78,310,391-78,520,604 SCAMP1, LHFPL2, 2 more genes
    nsv6566713inversion1nstd223human GRCh38 chr5: 78,403,157-78,403,735 , GRCh37.p13 chr5: 77,698,981-77,699,559 SCAMP1
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