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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv6984949copy number variation1nstd229human GRCh38 chr16: 67,595,901-67,645,100 , GRCh37.p13 chr16: 67,629,804-67,679,003 CTCF, CARMIL2
    nsv6980942copy number variation1nstd229human GRCh38 chr16: 67,645,356-67,645,405 , GRCh37.p13 chr16: 67,679,259-67,679,308 CARMIL2
    nsv6978989copy number variation1nstd229human GRCh38 chr16: 67,641,701-67,678,100 , GRCh37.p13 chr16: 67,675,604-67,712,003 ACD, PARD6A, 4 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6029673copy number variation1nstd212human GRCh38 chr16: 67,643,386-67,643,582 , GRCh37.p13 chr16: 67,677,289-67,677,485 CARMIL2
    nsv5980419copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,628,846-67,813,408 , GRCh38.p12 chr16: 67,594,943-67,779,505 CTCF, PARD6A, 6 more genes
    nsv5588771copy number variation1nstd207human GRCh38 chr16: 67,643,349-67,643,538 , GRCh37.p13 chr16: 67,677,252-67,677,441 CARMIL2
    nsv5272913copy number variation1nstd204human GRCh38.p13 chr16: 67,454,801-68,159,500 , GRCh37.p13 chr16: 67,488,704-68,193,403 EDC4, ATP6V0D1, 31 more genes
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    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
    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
    nsv4626983copy number variation1nstd183human GRCh37 chr16: 67,681,703-67,681,748 , GRCh38.p12 chr16: 67,647,800-67,647,845 CARMIL2
    nsv4624408copy number variation1nstd183human GRCh37 chr16: 67,681,703-67,681,833 , GRCh38.p12 chr16: 67,647,800-67,647,930 CARMIL2
    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
    nsv4350223copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,132,790-68,166,320 , GRCh38.p12 chr16: 67,098,887-68,132,417 CBFB, B3GNT9, 55 more genes
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