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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6734833copy number variation1nstd229human GRCh38 chr4: 52,020,519-52,022,958 , GRCh37.p13 chr4: 52,886,685-52,889,124 LRRC66, SGCB
    nsv6734307copy number variation1nstd229human GRCh38 chr4: 51,973,622-52,003,383 , GRCh37.p13 chr4: 52,839,788-52,869,549 RPL37AP2, LRRC66
    nsv6726311copy number variation1nstd229human GRCh38 chr4: 51,993,240-51,996,322 , GRCh37.p13 chr4: 52,859,406-52,862,488 LRRC66
    nsv6722176copy number variation1nstd229human GRCh38 chr4: 52,019,050-52,579,544 , GRCh37.p13 chr4: 52,885,216-53,445,710 SPATA18, SGCB, 5 more genes
    nsv6720828copy number variation1nstd229human GRCh38 chr4: 51,905,385-52,362,727 , GRCh37.p13 chr4: 52,771,551-53,228,893 RPL37AP2, DCUN1D4, 5 more genes
    nsv6719062copy number variation1nstd229human GRCh38 chr4: 51,975,689-52,000,118 , GRCh37.p13 chr4: 52,841,855-52,866,284 LRRC66, RPL37AP2
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6636293copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,886,015-53,451,495 , GRCh38.p12 chr4: 52,019,849-52,585,329 SPATA18, RNU6-1252P, 5 more genes
    nsv6629495copy number variation1nstd224human GRCh37 chr4: 52,706,270-53,122,932 , GRCh38.p12 chr4: 51,840,104-52,256,766 SGCB, DCUN1D4, 5 more genes
    nsv6390445copy number variation1nstd223human GRCh38 chr4: 51,993,238-51,996,329 , GRCh37.p13 chr4: 52,859,404-52,862,495 LRRC66
    nsv6384162copy number variation1nstd223human GRCh38 chr4: 52,002,459-52,003,297 , GRCh37.p13 chr4: 52,868,625-52,869,463 LRRC66
    nsv6381015copy number variation1nstd223human GRCh38 chr4: 52,008,826-52,009,378 , GRCh37.p13 chr4: 52,874,992-52,875,544 LRRC66
    nsv6377667copy number variation1nstd223human GRCh38 chr4: 52,008,501-52,010,100 , GRCh37.p13 chr4: 52,874,667-52,876,266 LRRC66
    nsv6377425copy number variation1nstd223human GRCh38 chr4: 51,999,659-52,000,319 , GRCh37.p13 chr4: 52,865,825-52,866,485 LRRC66
    nsv6376968copy number variation1nstd223human GRCh38 chr4: 52,015,701-52,018,800 , GRCh37.p13 chr4: 52,881,867-52,884,966 SGCB, LRRC66
    nsv6376937copy number variation1nstd223human GRCh38 chr4: 51,975,689-52,000,118 , GRCh37.p13 chr4: 52,841,855-52,866,284 RPL37AP2, LRRC66
    nsv6297353copy number variation1nstd186human GRCh37 chr4: 52,869,703-52,869,776 , GRCh38.p12 chr4: 52,003,537-52,003,610 LRRC66
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
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