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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074729inversion1nstd229human GRCh38 chr9: 86,127,872-86,128,111 , GRCh37.p13 chr9: 88,742,787-88,743,026 LOC101927623
    nsv7070278inversion1nstd229human GRCh38 chr9: 85,364,427-88,288,635 , GRCh37.p13 chr9: 87,979,342-90,903,550 LOC105376121, CTSL3P, 57 more genes
    nsv7069712inversion1nstd229human GRCh38 chr9: 85,876,416-87,369,299 , GRCh37.p13 chr9: 88,491,331-89,984,214 CDC20P1, C9orf153, 20 more genes
    nsv7068881inversion1nstd229human GRCh38 chr9: 85,364,378-88,276,332 , GRCh37.p13 chr9: 87,979,293-90,891,247 LOC100129202, LOC100287212, 57 more genes
    nsv7066081inversion1nstd229human GRCh38 chr9: 86,127,893-86,130,091 , GRCh37.p13 chr9: 88,742,808-88,745,006 LOC101927623
    nsv7064220inversion1nstd229human GRCh38 chr9: 86,136,819-86,140,969 , GRCh37.p13 chr9: 88,751,734-88,755,884 LOC101927623
    nsv7061453inversion1nstd229human GRCh38 chr9: 86,140,841-86,146,481 , GRCh37.p13 chr9: 88,755,756-88,761,396 LOC101927623
    nsv6871681copy number variation1nstd229human GRCh38 chr9: 86,127,873-86,130,090 , GRCh37.p13 chr9: 88,742,788-88,745,005 LOC101927623
    nsv6868756copy number variation1nstd229human GRCh38 chr9: 86,126,617-86,174,719 , GRCh37.p13 chr9: 88,741,532-88,789,634 LOC101927623, LOC100287212
    nsv6862211copy number variation1nstd229human GRCh38 chr9: 86,146,598-86,154,056 , GRCh37.p13 chr9: 88,761,513-88,768,971 LOC101927623
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633937copy number variation1nstd224human GRCh37 chr9: 88,756,246-88,842,933 , GRCh38.p12 chr9: 86,141,331-86,228,018 LOC101927623, C9orf153
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6564425inversion1nstd223human GRCh38 chr9: 86,051,015-86,392,968 , GRCh37.p13 chr9: 88,665,930-89,007,883 GOLM1, TUT7, 6 more genes
    nsv6562752inversion1nstd223human GRCh38 chr9: 86,051,014-86,393,052 , GRCh37.p13 chr9: 88,665,929-89,007,967 GOLM1, TUT7, 6 more genes
    nsv6439797copy number variation1nstd223human GRCh38 chr9: 86,127,871-86,130,089 , GRCh37.p13 chr9: 88,742,786-88,745,004 LOC101927623
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314204copy number variation1nstd102humanUncertain significance GRCh37 chr9: 87,881,345-88,749,247 , GRCh38.p12 chr9: 85,266,430-86,134,332 AGTPBP1, LOC105376121, 12 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
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