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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938313copy number variation1nstd209human GRCh38 chr16: 69,430,924-69,431,239 , GRCh37.p13 chr16: 69,464,827-69,465,142 CYB5B
    nsv5932770copy number variation1nstd209human GRCh38 chr16: 69,426,127-69,426,433 , GRCh37.p13 chr16: 69,460,030-69,460,336 CYB5B
    nsv5154339mobile element insertion1nstd203human GRCh38 chr16: 69,454,511-69,454,520 , GRCh37.p13 chr16: 69,488,414-69,488,423 CYB5B
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993205copy number variation1nstd200human GRCh38 chr16: 69,427,355-69,431,374 , GRCh37.p13 chr16: 69,461,258-69,465,277 CYB5B
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729943copy number variation1nstd102humanUncertain significance GRCh37 chr16: 69,369,131-69,942,990 , GRCh38.p12 chr16: 69,335,228-69,909,087 NIP7, CYB5B, 12 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv4506314mobile element insertion1nstd166human GRCh37.p13 chr16: 69,488,414-69,488,414 , GRCh38.p12 chr16: 69,454,511-69,454,511 CYB5B
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4321328inversion1nstd166human GRCh37.p13 chr16: 67,701,568-75,754,137 , GRCh38.p12 chr16: 67,667,665-75,720,239 , CDH3, 203 more genes
    nsv4247452copy number variation1nstd166human GRCh37.p13 chr16: 69,451,044-69,460,540 , GRCh38.p12 chr16: 69,417,141-69,426,637 CYB5B
    nsv4245984copy number variation1nstd166human GRCh37.p13 chr16: 69,465,000-69,474,000 , GRCh38.p12 chr16: 69,431,097-69,440,097 CYB5B
    nsv4244290copy number variation1nstd166human GRCh37.p13 chr16: 69,478,577-69,478,631 , GRCh38.p12 chr16: 69,444,674-69,444,728 LOC100420066, CYB5B
    nsv4242002copy number variation1nstd166human GRCh37.p13 chr16: 69,460,232-69,460,901 , GRCh38.p12 chr16: 69,426,329-69,426,998 CYB5B
    nsv4241778copy number variation1nstd166human GRCh37.p13 chr16: 69,499,663-69,501,238 , GRCh38.p12 chr16: 69,465,760-69,467,335 CYB5B
    nsv3922126copy number variation1nstd102humanPathogenic NCBI36 chr16: 67,644,861-81,865,787 , GRCh38 chr16: 69,053,457-83,274,681 , GRCh37 chr16: 69,087,360-83,308,286 LOC105371357, EXOSC6, 232 more genes
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