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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5938982copy number variation1nstd209human GRCh38 chr16: 57,745,294-57,745,343 , GRCh37.p13 chr16|NW_003871085.1: 5,185-5,234 , GRCh37.p13 chr16: 57,779,206-57,779,255 KATNB1
    nsv5937379copy number variation1nstd209human GRCh38 chr16: 57,734,145-57,734,320 , GRCh37.p13 chr16: 57,768,057-57,768,232 LOC107984852, KATNB1
    nsv5933650copy number variation1nstd209human GRCh38 chr16: 57,689,623-57,745,532 , GRCh37.p13 chr16: 57,723,535-57,774,021 KATNB1, DRC7, 3 more genes
    nsv5598107copy number variation1nstd207human GRCh38 chr16: 57,745,294-57,745,343 , GRCh37.p13 chr16|NW_003871085.1: 5,185-5,234 , GRCh37.p13 chr16: 57,779,206-57,779,255 KATNB1
    nsv5529732copy number variation1nstd206human GRCh38 chr16: 57,734,145-57,734,324 , GRCh37.p13 chr16: 57,768,057-57,768,236 LOC107984852, KATNB1
    nsv5147381mobile element insertion1nstd203human GRCh38 chr16: 57,742,090-57,742,103 , GRCh37.p13 chr16|NW_003871085.1: 1,981-1,994 , GRCh37.p13 chr16: 57,776,002-57,776,015 KATNB1
    nsv5140515mobile element insertion1nstd203human GRCh38 chr16: 57,745,344-57,745,344 , GRCh37.p13 chr16: 57,779,256-57,779,256 , GRCh37.p13 chr16|NW_003871085.1: 5,235-5,235 KATNB1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4743162copy number variation1nstd199human GRCh37 chr16: 57,779,221-57,779,273 , GRCh38.p12 chr16: 57,745,309-57,745,361 KATNB1
    nsv4729888copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,292,407-59,103,985 , GRCh38.p12 chr16: 57,258,495-59,070,081 HMGB3P32, DOK4, 57 more genes
    nsv4621880copy number variation1nstd183human GRCh37 chr16: 57,786,366-57,826,825 , GRCh38.p12 chr16: 57,752,454-57,792,913 MIR6772, KATNB1, 1 more genes
    nsv4578617copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,499,814-58,032,169 , GRCh38.p12 chr16: 57,465,902-57,998,265 HMGB3P32, KIFC3, 19 more genes
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4448191copy number variation1nstd175human GRCh37 chr16: 57,779,206-57,779,256 , GRCh38.p12 chr16: 57,745,294-57,745,344 KATNB1
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4418088copy number variation1nstd174human GRCh37 chr16: 57,779,257-57,779,307 , GRCh38.p12 chr16: 57,745,345-57,745,395 KATNB1
    nsv4367933copy number variation1nstd173human GRCh37 chr16: 55,822,788-62,090,267 , GRCh38.p12 chr16: 55,788,876-62,056,363 , RN7SL645P, 124 more genes
    nsv4233284copy number variation1nstd166human GRCh37.p13 chr16: 57,768,054-57,768,236 , GRCh38.p12 chr16: 57,734,142-57,734,324 KATNB1, LOC107984852
    nsv4233200copy number variation1nstd166human GRCh37.p13 chr16: 57,750,751-57,768,444 , GRCh38.p12 chr16: 57,716,839-57,734,532 KATNB1, DRC7, 1 more genes
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