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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143786copy number variation1nstd232human GRCh37.p13 chr16: 67,262,783-67,262,876 , GRCh38.p12 chr16: 67,228,880-67,228,973 TMEM208, FHOD1
    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
    nsv6989722copy number variation1nstd229human GRCh38 chr16: 67,228,585-67,249,444 , GRCh37.p13 chr16: 67,262,488-67,283,347 TMEM208, FHOD1, 1 more genes
    nsv6502683copy number variation1nstd223human GRCh38 chr16: 67,228,582-67,249,440 , GRCh37.p13 chr16: 67,262,485-67,283,343 FHOD1, SLC9A5, 1 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
    nsv5158635mobile element insertion1nstd203human GRCh38 chr16: 67,237,397-67,237,411 , GRCh37.p13 chr16: 67,271,300-67,271,314 FHOD1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993096copy number variation1nstd200human GRCh38 chr16: 67,235,984-67,236,082 , GRCh37.p13 chr16: 67,269,887-67,269,985 FHOD1
    nsv4993095copy number variation1nstd200human GRCh38 chr16: 67,228,585-67,249,440 , GRCh37.p13 chr16: 67,262,488-67,283,343 SLC9A5, TMEM208, 1 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857469copy number variation1nstd200human GRCh37 chr16: 67,269,887-67,269,985 , GRCh38.p12 chr16: 67,235,984-67,236,082 FHOD1
    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
    nsv4630558copy number variation1nstd183human GRCh37 chr16: 67,262,506-67,262,550 , GRCh38.p12 chr16: 67,228,603-67,228,647 FHOD1, TMEM208
    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
    nsv4423203copy number variation1nstd174human GRCh37 chr16: 67,175,101-67,323,199 , GRCh38.p12 chr16: 67,141,198-67,289,296 EXOC3L1, MIR328, 15 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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