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 527

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7094663copy number variation2nstd102humanPathogenic GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266 TPSP2, PRR25, 83 more genes
    nsv7094577copy number variation1nstd102humanUncertain significance GRCh37 chr16: 289,853-626,274 , GRCh38.p12 chr16: 239,854-576,274 ARHGDIG, DECR2, 17 more genes
    nsv7094575copy number variation1nstd102humanPathogenic GRCh37 chr16: 256,302-633,035 , GRCh38.p12 chr16: 206,303-583,035 FAM234A, RPL23AP5, 19 more genes
    nsv6977716copy number variation1nstd229human GRCh38 chr16: 246,437-249,971 , GRCh37.p13 chr16: 296,436-299,970 FAM234A
    nsv6975390copy number variation1nstd229human GRCh38 chr16: 267,621-267,737 , GRCh37.p13 chr16: 317,620-317,736 FAM234A, RGS11
    nsv6974722copy number variation1nstd229human GRCh38 chr16: 264,521-264,564 , GRCh37.p13 chr16: 314,520-314,563 FAM234A
    nsv6974697copy number variation1nstd229human GRCh38 chr16: 238,603-241,709 , GRCh37.p13 chr16: 288,602-291,708 FAM234A
    nsv6973486copy number variation1nstd229human GRCh38 chr16: 246,534-249,971 , GRCh37.p13 chr16: 296,533-299,970 FAM234A
    nsv6973295copy number variation1nstd229human GRCh38 chr16: 266,856-266,927 , GRCh37.p13 chr16: 316,855-316,926 FAM234A, RGS11
    nsv6972752copy number variation1nstd229human GRCh38 chr16: 269,466-271,263 , GRCh37.p13 chr16: 319,465-321,262 FAM234A, RGS11
    nsv6972599copy number variation1nstd229human GRCh38 chr16: 230,323-233,358 , GRCh37.p13 chr16: 280,322-283,357 FAM234A, C4orf46P1
    nsv6970909copy number variation1nstd229human GRCh38 chr16: 269,489-275,381 , GRCh37.p13 chr16: 319,488-325,381 RGS11, FAM234A
    nsv6970496copy number variation1nstd229human GRCh38 chr16: 263,479-265,038 , GRCh37.p13 chr16: 313,478-315,037 FAM234A
    nsv6969921copy number variation1nstd229human GRCh38 chr16: 251,098-259,058 , GRCh37.p13 chr16: 301,097-309,057 FAM234A
    nsv6967815copy number variation1nstd229human GRCh38 chr16: 251,401-267,300 , GRCh37.p13 chr16: 301,400-317,299 RGS11, FAM234A
    nsv6962097copy number variation1nstd229human GRCh38 chr16: 122,985-378,594 , GRCh37.p13 chr16: 172,984-428,594 MRPL28, HBA1, 16 more genes
    nsv6960536copy number variation1nstd229human GRCh38 chr16: 246,440-249,971 , GRCh37.p13 chr16: 296,439-299,970 FAM234A
    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