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Items: 1 to 20 of 263

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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
    nsv6971263copy number variation1nstd229human GRCh38 chr16: 2,473,701-2,501,800 , GRCh37.p13 chr16: 2,523,702-2,551,801 TBC1D24, NTN3
    nsv6967721copy number variation1nstd229human GRCh38 chr16: 2,468,801-2,476,400 , GRCh37.p13 chr16: 2,518,802-2,526,401 TBC1D24, NTN3
    nsv6967656copy number variation1nstd229human GRCh38 chr16: 2,465,690-2,470,193 , GRCh37.p13 chr16: 2,515,691-2,520,194 TEDC2-AS1, NTN3
    nsv6965906copy number variation1nstd229human GRCh38 chr16: 2,465,689-2,470,192 , GRCh37.p13 chr16: 2,515,690-2,520,193 TEDC2-AS1, NTN3
    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
    nsv6500868copy number variation1nstd223human GRCh38 chr16: 2,465,701-2,470,300 , GRCh37.p13 chr16: 2,515,702-2,520,301 NTN3, TEDC2-AS1
    nsv6498790copy number variation1nstd223human GRCh38 chr16: 2,334,094-2,648,283 , GRCh37.p13 chr16: 2,384,095-2,698,284 LOC105371050, NTN3, 16 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
    nsv6206618copy number variation1nstd214human GRCh38 chr16: 2,471,842-2,471,895 , GRCh37.p13 chr16: 2,521,843-2,521,896 NTN3
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133016copy number variation1nstd213human GRCh37 chr16: 2,450,000-2,590,001 , GRCh38.p12 chr16: 2,399,999-2,540,000 ATP6V0C, CCNF, 12 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
    nsv5946297copy number variation1nstd209human GRCh38 chr16: 2,471,842-2,471,895 , GRCh37.p13 chr16: 2,521,843-2,521,896 NTN3
    nsv5934013copy number variation1nstd209human GRCh38 chr16: 2,472,436-2,472,503 , GRCh37.p13 chr16: 2,522,437-2,522,504 NTN3
    nsv5520791copy number variation1nstd206human GRCh38 chr16: 2,472,436-2,472,513 , GRCh37.p13 chr16: 2,522,437-2,522,514 NTN3
    nsv5516299copy number variation1nstd206human GRCh38 chr16: 2,471,845-2,471,896 , GRCh37.p13 chr16: 2,521,846-2,521,897 NTN3
    nsv5380995copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978 TEDC2, MIR3677HG, 33 more genes
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