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Items: 1 to 20 of 131

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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
    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
    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
    nsv6398244copy number variation1nstd223human GRCh38 chr5: 78,359,601-78,360,800 , GRCh37.p13 chr5: 77,655,425-77,656,624 SCAMP1-AS1, SCAMP1
    nsv6396887copy number variation1nstd223human GRCh38 chr5: 78,346,301-78,411,300 , GRCh37.p13 chr5: 77,642,125-77,707,124 SCAMP1, SCAMP1-AS1
    nsv6313871copy number variation1nstd102humanUncertain significance GRCh37 chr5: 77,160,381-77,691,354 , GRCh38.p12 chr5: 77,864,557-78,395,530 TRQ-TTG7-1, AP3B1, 6 more genes
    nsv6244415mobile element insertion1nstd215human GRCh38 chr5: 78,358,363-78,358,363 , GRCh37.p13 chr5: 77,654,187-77,654,187 SCAMP1-AS1
    nsv6135683copy number variation1nstd213human GRCh37 chr5: 76,940,000-80,890,001 , GRCh38.p12 chr5: 77,644,175-81,594,182 ACTBP2, ARSB, 63 more genes
    nsv6135682copy number variation1nstd213human GRCh37 chr5: 76,540,000-78,280,001 , GRCh38.p12 chr5: 77,244,175-78,984,178 ACTBP2, ARSB, 17 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv6074272insertion1nstd212human GRCh38 chr5: 78,358,346-78,358,346 , GRCh37.p13 chr5: 77,654,170-77,654,170 SCAMP1-AS1
    nsv5966107insertion1nstd209human GRCh38 chr5: 78,358,345-78,358,345 , GRCh37.p13 chr5: 77,654,169-77,654,169 SCAMP1-AS1
    nsv5679243mobile element insertion2nstd211human GRCh38 chr5: 78,358,363-78,358,363 , GRCh37.p13 chr5: 77,654,187-77,654,187 SCAMP1-AS1
    nsv5673667copy number variation1nstd102humanPathogenic GRCh37 chr5: 77,385,207-78,135,259 , GRCh38.p12 chr5: 78,089,383-78,839,436 ARSB, AP3B1, 6 more genes
    nsv5642823insertion1nstd207human GRCh38 chr5: 78,358,345-78,358,345 , GRCh37.p13 chr5: 77,654,169-77,654,169 SCAMP1-AS1
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