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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144371copy number variation1nstd232human GRCh37.p13 chr16: 1,125,964-1,126,033 , GRCh38.p12 chr16: 1,075,964-1,076,033 SSTR5, SSTR5-AS1
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 more genes
    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
    nsv7073654inversion1nstd229human GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907 UBE2I, CRAMP1, 45 more genes
    nsv6977134copy number variation1nstd229human GRCh38 chr16: 951,401-1,472,200 , GRCh37.p13 chr16: 1,001,401-1,522,201 TPSG1, TPSAB1, 27 more genes
    nsv6975123copy number variation1nstd229human GRCh38 chr16: 1,022,081-1,209,212 , GRCh37.p13 chr16: 1,072,081-1,259,212 LOC105371042, CACNA1H, 4 more genes
    nsv6972122copy number variation1nstd229human GRCh38 chr16: 971,585-1,148,549 , GRCh37.p13 chr16: 1,021,585-1,198,549 LOC105371042, SOX8, 6 more genes
    nsv6971326copy number variation1nstd229human GRCh38 chr16: 1,021,295-1,072,645 , GRCh37.p13 chr16: 1,071,295-1,122,645 SSTR5, SSTR5-AS1
    nsv6970921copy number variation1nstd229human GRCh38 chr16: 1,008,520-1,148,078 , GRCh37.p13 chr16: 1,058,520-1,198,078 SSTR5-AS1, LOC107984906, 3 more genes
    nsv6970618copy number variation1nstd229human GRCh38 chr16: 1,072,013-1,072,043 , GRCh37.p13 chr16: 1,122,013-1,122,043 SSTR5-AS1, SSTR5
    nsv6970527copy number variation1nstd229human GRCh38 chr16: 1,073,138-1,091,910 , GRCh37.p13 chr16: 1,123,138-1,141,910 SSTR5-AS1, C1QTNF8, 1 more genes
    nsv6968307copy number variation1nstd229human GRCh38 chr16: 1,071,345-1,082,316 , GRCh37.p13 chr16: 1,121,345-1,132,316 SSTR5-AS1, SSTR5
    nsv6966910copy number variation1nstd229human GRCh38 chr16: 1,066,858-1,087,690 , GRCh37.p13 chr16: 1,116,858-1,137,690 SSTR5, C1QTNF8, 1 more genes
    nsv6637972copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185 MPG, LOC105371038, 78 more genes
    nsv6637768copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054 CRAMP1, LOC105371046, 57 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6623364copy number variation1nstd224human GRCh37 chr16: 1,079,582-1,134,818 , GRCh38.p12 chr16: 1,029,582-1,084,818 SSTR5-AS1, SSTR5
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