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 276

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130689insertion1nstd186human GRCh37 chr19: 53,694,248-53,694,283 , GRCh38.p12 chr19: 53,190,995-53,191,030 ZNF665
    nsv6129091copy number variation1nstd186human GRCh37 chr19: 53,688,342-53,692,984 , GRCh38.p12 chr19: 53,185,089-53,189,731 ZNF665
    nsv5978948inversion1nstd209human GRCh38 chr19: 52,690,058-53,366,131 , GRCh37.p13 chr19: 53,193,311-53,869,384 , NDUFV2P1, 34 more genes
    nsv5973180insertion1nstd209human GRCh38 chr19: 53,190,979-53,190,979 , GRCh37.p13 chr19: 53,694,232-53,694,232 ZNF665
    nsv5943784copy number variation1nstd209human GRCh38 chr19: 53,177,060-53,208,343 , GRCh37.p13 chr19: 53,680,313-53,711,596 ZNF665
    nsv5935137copy number variation1nstd209human GRCh38 chr19: 52,932,265-54,037,356 , GRCh37.p13 chr19: 53,435,518-54,528,887 LOC107987264, CACNG6, 113 more genes
    nsv5928805copy number variation1nstd209human GRCh38 chr19: 53,185,916-53,188,697 , GRCh37.p13 chr19: 53,689,169-53,691,950 ZNF665
    nsv5885722copy number variation1nstd209human GRCh38 chr19: 53,176,131-53,184,555 , GRCh37.p13 chr19: 53,679,384-53,687,808 ZNF665
    nsv5885121copy number variation1nstd209human GRCh38 chr19: 53,162,464-53,170,990 , GRCh37.p13 chr19: 53,665,717-53,674,243 ZNF665
    nsv5874530copy number variation1nstd209human GRCh38 chr19: 53,185,706-53,208,081 , GRCh37.p13 chr19: 53,688,959-53,711,334 ZNF665
    nsv5872736copy number variation2nstd209human GRCh38 chr19: 53,182,156-53,189,961 , GRCh37.p13 chr19: 53,685,409-53,693,214 ZNF665
    nsv5871332copy number variation1nstd209human GRCh38 chr19: 53,174,811-53,182,955 , GRCh37.p13 chr19: 53,678,064-53,686,208 ZNF665
    nsv5868704copy number variation1nstd209human GRCh38 chr19: 53,171,491-53,174,610 , GRCh37.p13 chr19: 53,674,744-53,677,863 ZNF665
    nsv5653822insertion1nstd207human GRCh38 chr19: 53,190,979-53,190,979 , GRCh37.p13 chr19: 53,694,232-53,694,232 ZNF665
    nsv5585958copy number variation1nstd207human GRCh38 chr19: 53,185,916-53,188,697 , GRCh37.p13 chr19: 53,689,169-53,691,950 ZNF665
    nsv5563403sequence alteration1nstd206human GRCh38 chr19: 52,689,727-53,366,381 , GRCh37.p13 chr19: 53,192,980-53,869,634 , ZNF28, 34 more genes
    nsv5545855insertion1nstd206human GRCh38 chr19: 53,190,995-53,191,030 , GRCh37.p13 chr19: 53,694,248-53,694,283 ZNF665
    nsv5532834copy number variation1nstd206human GRCh38 chr19: 53,177,060-53,208,348 , GRCh37.p13 chr19: 53,680,313-53,711,601 ZNF665
    nsv5532143copy number variation1nstd206human GRCh38 chr19: 53,050,850-53,442,009 , GRCh37.p13 chr19: 53,554,103-53,945,262 RPL39P36, FAM90A27P, 24 more genes
    nsv5528776copy number variation1nstd206human GRCh38 chr19: 53,182,031-53,182,121 , GRCh37.p13 chr19: 53,685,284-53,685,374 ZNF665
    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