U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 88

    loading data ...

    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
    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
    nsv5270819copy number variation1nstd204human GRCh38.p13 chr16: 57,333,209-57,368,995 , GRCh37.p13 chr16: 57,367,121-57,402,907 CCL22
    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
    nsv4864167copy number variation1nstd200human GRCh37 chr16: 56,805,348-57,545,260 , GRCh38.p12 chr16: 56,771,436-57,511,348 , POLR2C, 24 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
    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
    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
    nsv3916542copy number variation1nstd102humanPathogenic GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526 CES1, SNORA46, 139 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 CFAP69P1, GAS8-AS1, 716 more genes
    nsv3915341copy number variation1nstd102humanBenign 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 GINS3, LINC00919, 985 more genes
    nsv3915118copy number variation1nstd102humanBenign 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 ZFHX3, CENPN-AS1, 985 more genes
    nsv3913084copy number variation1nstd102humanPathogenic NCBI36 chr16: 55,475,005-69,871,379 , GRCh38 chr16: 56,883,592-71,279,975 , GRCh37 chr16: 56,917,504-71,313,878 MIR6773, ATP6V0D1, 280 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center