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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5015162copy number variation1nstd200human GRCh38 chr16: 89,919,801-89,920,802 , GRCh37.p13 chr16: 89,986,209-89,987,210 TUBB3, MC1R
    nsv5013597copy number variation1nstd200human GRCh38 chr16: 89,889,333-89,922,309 , GRCh37.p13 chr16: 89,955,741-89,988,717 TUBB3, MC1R, 1 more genes
    nsv4864399copy number variation1nstd200human GRCh37 chr16: 89,955,741-89,988,717 , GRCh38.p12 chr16: 89,889,333-89,922,309 TUBB3, TCF25, 1 more genes
    nsv4729945copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,222,732-90,155,062 , GRCh38.p12 chr16: 88,189,126-90,088,654 SNORD68, LOC105371412, 75 more genes
    nsv4729883copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,499,489-90,125,146 , GRCh38.p12 chr16: 89,433,081-90,058,738 DBNDD1, RNU6-430P, 32 more genes
    nsv4729842copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,156,662-90,023,446 , GRCh38.p12 chr16: 89,090,254-89,957,038 ZNF778, SPATA2L, 33 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
    nsv4682705copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,804,999-89,986,630 , GRCh38.p12 chr16: 89,738,591-89,920,222 FANCA, MC1R, 5 more genes
    nsv4682652copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,985,667-89,986,620 , GRCh38.p12 chr16: 89,919,259-89,920,212 MC1R, TUBB3
    nsv4681959copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,986,207-89,987,210 , GRCh38 chr16: 89,919,799-89,920,802 MC1R, TUBB3
    nsv4681449copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,845,199-89,986,630 , GRCh38.p12 chr16: 89,778,791-89,920,222 TCF25, MC1R, 4 more genes
    nsv4626262copy number variation2nstd183human GRCh37 chr16: 89,933,271-90,104,099 , GRCh38.p12 chr16: 89,866,863-90,037,691 GAS8, CENPBD1P, 10 more genes
    nsv4622665copy number variation2nstd183human GRCh37 chr16: 89,916,362-90,105,215 , GRCh38.p12 chr16: 89,849,954-90,038,807 , CENPBD1P, 12 more genes
    nsv4531834copy number variation1nstd166human GRCh37.p13 chr16: 89,978,999-90,161,500 , GRCh38.p12 chr16: 89,912,591-90,095,092 AFG3L1P, TUBB8P7, 10 more genes
    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
    nsv4414559copy number variation1nstd174human GRCh37 chr16: 89,923,906-90,103,659 , GRCh38.p12 chr16: 89,857,498-90,037,251 SNORA119, AFG3L1P, 10 more genes
    nsv4371851copy number variation1nstd173human GRCh37 chr16: 89,955,902-89,991,079 , GRCh38.p12 chr16: 89,889,494-89,924,671 TUBB3, MC1R, 1 more genes
    nsv4371164copy number variation1nstd173human GRCh37 chr16: 89,956,613-89,991,079 , GRCh38.p12 chr16: 89,890,205-89,924,671 MC1R, TCF25, 1 more genes
    nsv4367671copy number variation1nstd173human GRCh37 chr16: 89,956,642-89,991,079 , GRCh38.p12 chr16: 89,890,234-89,924,671 TCF25, MC1R, 1 more genes
    nsv4349253copy number variation1nstd102humanPathogenic GRCh37 chr16: 82,761,333-90,055,381 , GRCh38.p12 chr16: 82,727,728-89,988,973 RN7SL134P, CDK10, 178 more genes
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