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Items: 1 to 20 of 507

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6971914copy number variation1nstd229human GRCh38 chr16: 1,096,101-1,099,700 , GRCh37.p13 chr16: 1,146,101-1,149,700 C1QTNF8
    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
    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
    nsv6969365copy number variation1nstd229human GRCh38 chr16: 1,093,487-1,093,647 , GRCh37.p13 chr16: 1,143,487-1,143,647 C1QTNF8
    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
    nsv6961104copy number variation1nstd229human GRCh38 chr16: 1,088,411-1,125,921 , GRCh37.p13 chr16: 1,138,411-1,175,921 LOC107984906, C1QTNF8, 1 more genes
    nsv6960250copy number variation1nstd229human GRCh38 chr16: 1,096,300-1,128,018 , GRCh37.p13 chr16: 1,146,300-1,178,018 C1QTNF8, LOC105371042, 1 more genes
    nsv6958508copy number variation1nstd229human GRCh38 chr16: 1,090,308-1,094,858 , GRCh37.p13 chr16: 1,140,308-1,144,858 C1QTNF8
    nsv6958089copy number variation1nstd229human GRCh38 chr16: 1,091,757-1,095,175 , GRCh37.p13 chr16: 1,141,757-1,145,175 C1QTNF8
    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
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