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Items: 1 to 20 of 134

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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
    nsv5931914copy number variation1nstd209human GRCh38 chr19: 53,672,928-53,819,237 , GRCh37.p13 chr19: 54,176,182-54,322,491 MIR516B2, MIR520D, 56 more genes
    nsv5882732copy number variation2nstd209human GRCh38 chr19: 53,700,087-53,701,086 , GRCh37.p13 chr19: 54,203,341-54,204,340 MIR518B, MIR518F, 2 more genes
    nsv5877652copy number variation1nstd209human GRCh38 chr19: 53,700,088-53,707,345 , GRCh37.p13 chr19: 54,203,342-54,210,599 MIR518F, MIR520B, 5 more genes
    nsv5329031copy number variation1nstd204human GRCh37.p13 chr19: 54,201,512-54,204,303 , GRCh38.p13 chr19: 53,698,258-53,701,049 MIR523, MIR518F, 3 more genes
    nsv5295815copy number variation1nstd204human GRCh38.p13 chr19: 53,698,301-53,701,100 , GRCh37.p13 chr19: 54,201,555-54,204,354 MIR520B, MIR523, 3 more genes
    nsv5024894copy number variation1nstd200human GRCh38 chr19: 53,672,928-53,819,261 , GRCh37.p13 chr19: 54,176,182-54,322,515 MIR515-1, MIR1283-1, 56 more genes
    nsv5024885copy number variation1nstd200human GRCh38 chr19: 53,512,116-53,707,321 , GRCh37.p13 chr19: 54,015,370-54,210,575 MIR518B, MIR518C, 30 more genes
    nsv5021264copy number variation1nstd200human GRCh38 chr19: 53,698,299-53,699,887 , GRCh37.p13 chr19: 54,201,553-54,203,141 MIR523, LOC107985346, 2 more genes
    nsv5021261copy number variation1nstd200human GRCh38 chr19: 53,681,734-53,713,205 , GRCh37.p13 chr19: 54,184,988-54,216,459 MIR525, MIR520A, 17 more genes
    nsv4865300copy number variation1nstd200human GRCh37 chr19: 54,015,370-54,210,575 , GRCh38.p12 chr19: 53,512,116-53,707,321 RNU6-698P, LOC107985342, 30 more genes
    nsv4853553copy number variation1nstd200human GRCh37 chr19: 54,201,539-54,204,282 , GRCh38.p12 chr19: 53,698,285-53,701,028 MIR518B, MIR523, 3 more genes
    nsv4853552copy number variation1nstd200human GRCh37 chr19: 54,201,569-54,203,119 , GRCh38.p12 chr19: 53,698,315-53,699,865 LOC107985346, MIR518F, 2 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
    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
    nsv4623997copy number variation1nstd183human GRCh37 chr19: 54,042,427-54,261,320 , GRCh38.p12 chr19: 53,539,173-53,758,066 RNU6-698P, MIR518A2, 56 more genes
    nsv4436464copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,039,784-54,484,439 , GRCh38 chr19: 53,536,530-53,981,185 MIR1283-2, MIR515-1, 74 more genes
    nsv4417845copy number variation1nstd174human GRCh37 chr19: 54,033,686-54,229,395 , GRCh38.p12 chr19: 53,530,432-53,726,141 MIR512-2, MIR515-1, 40 more genes
    nsv4378526copy number variation1nstd173human GRCh37 chr19: 54,175,131-54,318,410 , GRCh38.p12 chr19: 53,671,877-53,815,156 MIR516B2, MIR515-1, 57 more genes
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