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Items: 1 to 20 of 417

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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
    nsv7094763copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,034,220-2,152,787 , GRCh38.p12 chr16: 1,984,219-2,102,786 NHERF2, PKD1-AS1, 10 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
    nsv7066398inversion1nstd229human GRCh38 chr16: 1,795,672-2,006,533 , GRCh37.p13 chr16: 1,845,673-2,056,534 LINC00254, HAGH, 18 more genes
    nsv6977037copy number variation1nstd229human GRCh38 chr16: 1,683,908-2,006,596 , GRCh37.p13 chr16: 1,733,909-2,056,597 RPS2, SNORA78, 28 more genes
    nsv6971016copy number variation1nstd229human GRCh38 chr16: 1,949,201-2,138,200 , GRCh37.p13 chr16: 1,999,202-2,188,201 MIR4516, NTHL1, 22 more genes
    nsv6965228copy number variation1nstd229human GRCh38 chr16: 2,002,998-2,028,660 , GRCh37.p13 chr16: 2,052,999-2,078,661 RN7SL219P, ZNF598, 2 more genes
    nsv6963240copy number variation1nstd229human GRCh38 chr16: 2,003,288-2,003,398 , GRCh37.p13 chr16: 2,053,289-2,053,399 ZNF598
    nsv6961258copy number variation1nstd229human GRCh38 chr16: 1,796,554-2,140,440 , GRCh37.p13 chr16: 1,846,555-2,190,441 NTHL1, MSRB1, 29 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
    nsv6637964copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,146,432 , GRCh38.p12 chr16: 1,971,143-2,096,431 NTHL1, SYNGR3, 11 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
    nsv6595307inversion1nstd223human GRCh38 chr16: 1,516,512-2,069,676 , GRCh37.p13 chr16: 1,566,513-2,119,677 MAPK8IP3-AS1, EME2, 37 more genes
    nsv6512027copy number variation1nstd223human GRCh38 chr16: 2,006,038-2,006,795 , GRCh37.p13 chr16: 2,056,039-2,056,796 ZNF598
    nsv6509607copy number variation1nstd223human GRCh38 chr16: 2,000,752-2,012,914 , GRCh37.p13 chr16: 2,050,753-2,062,915 RN7SL219P, ZNF598
    nsv6315059copy number variation1nstd102humanPathogenic GRCh38 chr16: 1,903,155-2,093,402 , GRCh37.p13 chr16: 1,953,156-2,143,403 NPW, HS3ST6, 21 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
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