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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7148035insertion1nstd232human GRCh37.p13 chr3: 98,236,033-98,236,033 , GRCh38.p12 chr3: 98,517,189-98,517,189 CLDND1
    nsv7047168inversion1nstd229human GRCh38 chr3: 98,270,010-99,398,075 , GRCh37.p13 chr3: 97,988,854-99,116,919 OR5K2, RPL38P4, 24 more genes
    nsv7046246inversion1nstd229human GRCh38 chr3: 98,222,641-99,359,746 , GRCh37.p13 chr3: 97,941,485-99,078,590 LOC105374004, UBFD1P1, 28 more genes
    nsv7041727inversion1nstd229human GRCh38 chr3: 94,070,424-99,088,195 , GRCh37.p13 chr3: 93,789,268-98,807,039 LINC00973, OR5H7P, 63 more genes
    nsv7038494inversion1nstd229human GRCh38 chr3: 98,359,390-99,063,927 , GRCh37.p13 chr3: 98,078,234-98,782,771 CLDND1, DCBLD2, 17 more genes
    nsv6716356copy number variation1nstd229human GRCh38 chr3: 98,517,663-98,518,250 , GRCh37.p13 chr3: 98,236,507-98,237,094 CLDND1
    nsv6715314copy number variation1nstd229human GRCh38 chr3: 98,520,282-98,520,412 , GRCh37.p13 chr3: 98,239,126-98,239,256 CLDND1
    nsv6712762copy number variation1nstd229human GRCh38 chr3: 96,620,998-98,689,220 , GRCh37.p13 chr3: 96,339,842-98,408,064 GPR15, OR5K1, 41 more genes
    nsv6710519copy number variation1nstd229human GRCh38 chr3: 98,519,494-98,643,402 , GRCh37.p13 chr3: 98,238,338-98,362,246 CLDND1, CPOX, 3 more genes
    nsv6709547copy number variation1nstd229human GRCh38 chr3: 98,488,607-99,037,059 , GRCh37.p13 chr3: 98,207,451-98,755,903 RNU6-26P, WWP1P1, 13 more genes
    nsv6698611copy number variation1nstd229human GRCh38 chr3: 98,521,157-98,521,499 , GRCh37.p13 chr3: 98,240,001-98,240,343 CLDND1
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6368382copy number variation1nstd223human GRCh38 chr3: 98,494,301-98,810,500 , GRCh37.p13 chr3: 98,213,145-98,529,344 PDLIM1P4, CPOX, 10 more genes
    nsv6367194copy number variation1nstd223human GRCh38 chr3: 98,488,607-99,037,059 , GRCh37.p13 chr3: 98,207,451-98,755,903 GPR15, LINC00973, 13 more genes
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4914539copy number variation1nstd200human GRCh38 chr3: 98,517,663-98,518,252 , GRCh37.p13 chr3: 98,236,507-98,237,096 CLDND1
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