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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935137copy number variation1nstd209human GRCh38 chr19: 52,932,265-54,037,356 , GRCh37.p13 chr19: 53,435,518-54,528,887 LOC107987264, CACNG6, 113 more genes
    nsv5931037copy number variation1nstd209human GRCh38 chr19: 53,760,924-54,051,285 , GRCh37.p13 chr19: 54,264,178-54,528,887 CACNG6, HMGN1P32, 17 more genes
    nsv5928919copy number variation1nstd209human GRCh38 chr19: 53,852,686-53,866,384 , GRCh37.p13 chr19: 54,355,940-54,369,638 MYADM-AS1, MYADM
    nsv5882524copy number variation1nstd209human GRCh38 chr19: 53,860,722-53,866,377 , GRCh37.p13 chr19: 54,363,976-54,369,631 MYADM, MYADM-AS1
    nsv5599972copy number variation1nstd207human GRCh38 chr19: 53,869,971-53,870,233 , GRCh37.p13 chr19: 54,373,225-54,373,487 MYADM, MYADM-AS1
    nsv5522356copy number variation1nstd206human GRCh38 chr19: 53,852,691-53,866,385 , GRCh37.p13 chr19: 54,355,945-54,369,639 MYADM, MYADM-AS1
    nsv5518412copy number variation1nstd206human GRCh38 chr19: 53,862,701-53,866,208 , GRCh37.p13 chr19: 54,365,955-54,369,462 MYADM, MYADM-AS1
    nsv5381201copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,297,303-54,410,149 , GRCh38.p12 chr19: 53,794,049-53,906,895 MYADM-AS1, MYADM, 2 more genes
    nsv5359936translocation1nstd200human GRCh38 chr19: 53,866,385-53,866,385 , GRCh38 chr19: 53,852,691-53,852,691 , GRCh37.p13 chr19: 54,355,945-54,355,945 , GRCh37.p13 chr19: 54,369,639-54,369,639 MYADM-AS1, MYADM
    nsv5021297copy number variation1nstd200human GRCh38 chr19: 53,862,701-53,866,208 , GRCh37.p13 chr19: 54,365,955-54,369,462 MYADM-AS1, MYADM
    nsv4853577copy number variation1nstd200human GRCh37 chr19: 54,355,945-54,369,639 , GRCh38.p12 chr19: 53,852,691-53,866,385 MYADM-AS1, MYADM
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4683322copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,376,784-54,396,645 , GRCh38.p12 chr19: 53,873,530-53,893,391 PRKCG, MYADM
    nsv4667346copy number variation1nstd186human GRCh37 chr19: 54,355,925-54,369,626 , GRCh38.p12 chr19: 53,852,671-53,866,372 MYADM-AS1, MYADM
    nsv4630282copy number variation1nstd183human GRCh37 chr19: 54,024,640-54,370,843 , GRCh38.p12 chr19: 53,521,386-53,867,589 MIR519A2, MIR518D, 70 more genes
    nsv4628647copy number variation1nstd183human GRCh37 chr19: 54,355,925-54,369,626 , GRCh38.p12 chr19: 53,852,671-53,866,372 MYADM-AS1, MYADM
    nsv4623560copy number variation1nstd183human GRCh37 chr19: 54,358,171-54,369,544 , GRCh38.p12 chr19: 53,854,917-53,866,290 MYADM, MYADM-AS1
    nsv4619407copy number variation2nstd183human GRCh37 chr19: 54,356,155-54,369,469 , GRCh38.p12 chr19: 53,852,901-53,866,215 MYADM-AS1, MYADM
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