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Items: 1 to 20 of 86

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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
    nsv5531313copy number variation1nstd206human GRCh38 chr16: 57,369,294-57,370,868 , GRCh37.p13 chr16: 57,403,206-57,404,780 CX3CL1
    nsv5301175copy number variation1nstd204human GRCh38.p13 chr16: 56,771,413-57,511,371 , GRCh37.p13 chr16: 56,805,325-57,545,283 , PLLP, 24 more genes
    nsv5276145copy number variation1nstd204human GRCh38.p13 chr16: 57,381,395-57,382,394 , GRCh37.p13 chr16: 57,415,307-57,416,306 CX3CL1
    nsv5269564copy number variation1nstd204human GRCh38.p13 chr16: 57,352,392-57,430,089 , GRCh37.p13 chr16: 57,386,304-57,464,001 CX3CL1, CIAPIN1, 2 more genes
    nsv5263209copy number variation1nstd204human GRCh38.p13 chr16: 56,771,401-57,423,100 , GRCh37.p13 chr16: 56,805,313-57,457,012 , NUP93, 19 more genes
    nsv5008395copy number variation1nstd200human GRCh38 chr16: 57,384,879-57,389,968 , GRCh37.p13 chr16: 57,418,791-57,423,880 CX3CL1
    nsv5008394copy number variation1nstd200human GRCh38 chr16: 57,369,256-57,379,803 , GRCh37.p13 chr16: 57,403,168-57,413,715 CX3CL1
    nsv4864167copy number variation1nstd200human GRCh37 chr16: 56,805,348-57,545,260 , GRCh38.p12 chr16: 56,771,436-57,511,348 , POLR2C, 24 more genes
    nsv4857212copy number variation1nstd200human GRCh37 chr16: 57,418,791-57,423,880 , GRCh38.p12 chr16: 57,384,879-57,389,968 CX3CL1
    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
    nsv4532000copy number variation1nstd166human GRCh37.p13 chr16: 57,404,165-57,404,823 , GRCh38.p12 chr16: 57,370,253-57,370,911 CX3CL1
    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
    nsv4367933copy number variation1nstd173human GRCh37 chr16: 55,822,788-62,090,267 , GRCh38.p12 chr16: 55,788,876-62,056,363 , RN7SL645P, 124 more genes
    nsv3963979copy number variation1nstd168human GRCh38 chr16: 57,372,088-57,387,259 , GRCh37.p13 chr16: 57,406,000-57,421,171 CX3CL1
    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
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