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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046399inversion1nstd229human GRCh38 chr7: 66,773-207,605 , GRCh37.p13 chr7: 66,773-207,605 LOC101929756, LOC105375115, 6 more genes
    nsv7040734inversion1nstd229human GRCh38 chr7: 85,903-185,404 , GRCh37.p13 chr7: 85,903-185,404 LINC03014, LOC105375115, 3 more genes
    nsv6817371copy number variation1nstd229human GRCh38 chr7: 133,183-169,689 , GRCh37.p13 chr7: 133,183-169,689 LINC03015, LINC03014
    nsv6816123copy number variation1nstd229human GRCh38 chr7: 45,102-189,606 , GRCh37.p13 chr7: 45,102-189,606 LINC03015, LOC105375115, 5 more genes
    nsv6815218copy number variation1nstd229human GRCh38 chr7: 83,059-332,901 , GRCh37.p13 chr7: 83,059-372,867 LOC105375114, LOC105375115, 8 more genes
    nsv6814472copy number variation1nstd229human GRCh38 chr7: 132,470-269,451 , GRCh37.p13 chr7: 132,470-309,417 LOC105375115, LOC105375116, 3 more genes
    nsv6813892copy number variation1nstd229human GRCh38 chr7: 114,301-183,400 , GRCh37.p13 chr7: 114,301-183,400 LOC105375116, LINC03015, 3 more genes
    nsv6813105copy number variation1nstd229human GRCh38 chr7: 113,648-211,103 , GRCh37.p13 chr7: 113,648-211,103 LOC105375114, LOC105375115, 4 more genes
    nsv6809847copy number variation1nstd229human GRCh38 chr7: 122,548-292,439 , GRCh37.p13 chr7: 122,548-332,405 FOXL3, LOC105375115, 5 more genes
    nsv6807441copy number variation1nstd229human GRCh38 chr7: 64,763-302,139 , GRCh37.p13 chr7: 64,763-342,105 LINC03015, LOC101929756, 8 more genes
    nsv6805656copy number variation1nstd229human GRCh38 chr7: 66,663-287,397 , GRCh37.p13 chr7: 66,663-327,363 LOC105375116, FAM20C, 6 more genes
    nsv6805636copy number variation1nstd229human GRCh38 chr7: 136,919-236,389 , GRCh37.p13 chr7: 136,919-232,484 LOC105375115, LINC03015, 3 more genes
    nsv6805582copy number variation1nstd229human GRCh38 chr7: 139,905-146,573 , GRCh37.p13 chr7: 139,905-146,573 LINC03015
    nsv6804682copy number variation1nstd229human GRCh38 chr7: 118,001-183,400 , GRCh37.p13 chr7: 118,001-183,400 LOC105375115, LINC03014, 3 more genes
    nsv6804511copy number variation1nstd229human GRCh38 chr7: 86,792-257,444 , GRCh37.p13 chr7: 86,792-297,410 LOC105375115, FAM20C, 4 more genes
    nsv6801341copy number variation1nstd229human GRCh38 chr7: 120,225-151,138 , GRCh37.p13 chr7: 120,225-151,138 LINC03015, LINC03014, 1 more genes
    nsv6798924copy number variation1nstd229human GRCh38 chr7: 62,603-248,832 , GRCh37.p13 chr7: 62,603-288,798 LOC105375115, LOC101929756, 6 more genes
    nsv6636881copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,361-704,573 , GRCh38.p12 chr7: 43,361-664,936 LOC116435278, LOC105375115, 18 more genes
    nsv6634885copy number variation1nstd227human GRCh37 chr7: 44,935-194,247 , GRCh38.p12 chr7: 44,935-194,247 , GRCh38.p12 chr7|NT_187558.1: 1,034-153,651 , GRCh38.p12 chr7|NT_187653.1: 37,256-186,568 FAM20C, LINC03014, 6 more genes
    nsv6634750copy number variation1nstd227human GRCh37 chr7: 123,956-198,903 , GRCh38.p12 chr7: 123,956-198,903 , GRCh38.p12 chr7|NT_187558.1: 79,877-157,952 , GRCh38.p12 chr7|NT_187653.1: 116,277-190,869 FAM20C, LINC03014, 3 more genes
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