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    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
    nsv7066288inversion1nstd229human GRCh38 chr16: 2,148,442-2,148,497 , GRCh37.p13 chr16: 2,198,443-2,198,498 RAB26
    nsv6972479copy number variation1nstd229human GRCh38 chr16: 2,152,044-2,152,109 , GRCh37.p13 chr16: 2,202,045-2,202,110 RAB26
    nsv6960558copy number variation1nstd229human GRCh38 chr16: 2,151,269-2,158,797 , GRCh37.p13 chr16: 2,201,270-2,208,798 SNHG19, TRAF7, 2 more genes
    nsv6959573copy number variation1nstd229human GRCh38 chr16: 2,150,055-2,153,781 , GRCh37.p13 chr16: 2,200,056-2,203,782 SNHG19, RAB26, 2 more genes
    nsv6959164copy number variation1nstd229human GRCh38 chr16: 1,882,476-2,224,508 , GRCh37.p13 chr16: 1,932,477-2,274,509 SNORD60, NTHL1, 35 more genes
    nsv6958935copy number variation1nstd229human GRCh38 chr16: 1,975,501-2,237,700 , GRCh37.p13 chr16: 2,025,502-2,287,701 BRICD5, MLST8, 25 more genes
    nsv6638000copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 2,106,895-2,227,470 , GRCh38.p12 chr16: 2,056,894-2,177,469 PKD1, TSC2, 10 more genes
    nsv6637664copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,266,791 , GRCh38.p12 chr16: 1,971,143-2,216,790 SNHG19, MIR6511B1, 22 more genes
    nsv6637330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,942,430-2,653,144 , GRCh38.p12 chr16: 1,892,429-2,603,143 SNHG19, SNHG9, 58 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
    nsv6315012copy number variation1nstd102humanPathogenic GRCh38 chr16: 2,066,081-2,241,220 , GRCh37.p13 chr16: 2,116,082-2,291,221 CASKIN1, PKD1, 16 more genes
    nsv6315010copy number variation1nstd102humanPathogenic GRCh38 chr16: 2,047,157-2,220,112 , GRCh37.p13 chr16: 2,097,158-2,270,113 RAB26, BRICD5, 14 more genes
    nsv6314182copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,847,662-2,653,144 , GRCh38.p12 chr16: 1,797,661-2,603,143 CASKIN1, RPL3L, 63 more genes
    nsv6291471copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,830,141-2,592,737 , GRCh38.p12 chr16: 1,780,140-2,542,736 CEMP1, NTN3, 65 more genes
    nsv6274978copy number variation1nstd214human GRCh38 chr16: 2,152,041-2,152,108 , GRCh37.p13 chr16: 2,202,042-2,202,109 RAB26
    nsv6133285copy number variation1nstd213human GRCh37 chr16: 850,000-2,500,001 , GRCh38.p12 chr16: 800,000-2,450,000 ABCA3, CCNF, 101 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5941257copy number variation1nstd209human GRCh38 chr16: 2,152,041-2,152,108 , GRCh37.p13 chr16: 2,202,042-2,202,109 RAB26
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