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Items: 1 to 20 of 141

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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
    nsv5931428copy number variation1nstd209human GRCh38 chr16: 58,011,547-58,011,640 , GRCh37.p13 chr16: 58,045,451-58,045,544 USB1
    nsv5530006copy number variation1nstd206human GRCh38 chr16: 58,007,232-58,043,361 , GRCh37.p13 chr16: 58,041,136-58,077,265 USB1, MMP15
    nsv5008418copy number variation1nstd200human GRCh38 chr16: 58,001,931-58,002,009 , GRCh37.p13 chr16: 58,035,835-58,035,913 USB1
    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
    nsv4532653copy number variation1nstd166human GRCh37.p13 chr16: 58,035,835-58,035,913 , GRCh38.p12 chr16: 58,001,931-58,002,009 USB1
    nsv4507522mobile element insertion1nstd166human GRCh37.p13 chr16: 58,042,167-58,042,167 , GRCh38.p12 chr16: 58,008,263-58,008,263 USB1
    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
    nsv4420098copy number variation1nstd174human GRCh37 chr16: 58,054,177-58,054,604 , GRCh38.p12 chr16: 58,020,273-58,020,700 USB1
    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
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CDH16, TP53TG3HP, 968 more genes
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