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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942007copy number variation1nstd209human GRCh38 chr19: 39,321,141-39,321,453 , GRCh37.p13 chr19: 39,811,781-39,812,093 LRFN1
    nsv5709474mobile element insertion2nstd211human GRCh38 chr19: 39,316,167-39,316,167 , GRCh37.p13 chr19: 39,806,807-39,806,807 LRFN1
    nsv5423744mobile element insertion1nstd206human GRCh38 chr19: 39,316,167-39,316,218 , GRCh37.p13 chr19: 39,806,807-39,806,858 LRFN1
    nsv5173532mobile element insertion1nstd203human GRCh38 chr19: 39,316,151-39,316,167 , GRCh37.p13 chr19: 39,806,791-39,806,807 LRFN1
    nsv4759259insertion1nstd199human GRCh37 chr19: 39,806,802-39,806,802 , GRCh38.p12 chr19: 39,316,162-39,316,162 LRFN1
    nsv4628819copy number variation1nstd183human GRCh37 chr19: 39,811,570-39,886,212 , GRCh38.p12 chr19: 39,320,930-39,395,572 GMFG, PAF1, 4 more genes
    nsv4505726mobile element insertion1nstd166human GRCh37.p13 chr19: 39,806,791-39,806,791 , GRCh38.p12 chr19: 39,316,151-39,316,151 LRFN1
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3912394copy number variation1nstd102humanUncertain significance NCBI36 chr19: 44,054,509-44,534,649 , GRCh37.p13 chr19: 39,362,669-39,842,809 , GRCh38.p12 chr19: 38,872,029-39,352,169 SAMD4B, IFNL1, 20 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
    nsv2752158copy number variation1nstd130human GRCh37 chr19: 289,244-58,996,454 , GRCh38.p12 chr19: 289,244-58,485,087 , NFKBIB, 2456 more genes
    nsv1958685short tandem repeat1nstd128human GRCh37 chr19: 39,811,106-39,811,129 , GRCh38.p12 chr19: 39,320,466-39,320,489 LRFN1
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