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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv7068931inversion1nstd229human GRCh38 chr16: 57,985,556-58,064,777 , GRCh37.p13 chr16: 58,019,460-58,098,681 MMP15, ZNF319, 2 more genes
    nsv6986069copy number variation1nstd229human GRCh38 chr16: 57,985,601-58,048,500 , GRCh37.p13 chr16: 58,019,505-58,082,404 USB1, MMP15, 2 more genes
    nsv6982771copy number variation1nstd229human GRCh38 chr16: 57,866,158-58,046,118 , GRCh37.p13 chr16: 57,900,062-58,080,022 MMP15, USB1, 3 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6498884copy number variation1nstd223human GRCh38 chr16: 57,990,116-57,992,888 , GRCh37.p13 chr16: 58,024,020-58,026,792 ZNF319
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    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
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    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
    nsv4619360copy number variation1nstd183human GRCh37 chr16: 58,034,054-58,034,733 , GRCh38.p12 chr16: 58,000,150-58,000,829 USB1, ZNF319
    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
    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
    nsv4371719copy number variation1nstd173human GRCh37 chr16: 57,869,458-58,053,161 , GRCh38.p12 chr16: 57,835,554-58,019,257 ZNF319, KIFC3, 3 more genes
    nsv4367933copy number variation1nstd173human GRCh37 chr16: 55,822,788-62,090,267 , GRCh38.p12 chr16: 55,788,876-62,056,363 , RN7SL645P, 124 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
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