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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935669copy number variation1nstd209human GRCh38 chr19: 49,049,441-49,056,063 , GRCh37.p13 chr19: 49,552,698-49,559,320 CGB7, CGB8, 1 more genes
    nsv5881117copy number variation1nstd209human GRCh38 chr19: 49,049,428-49,055,008 , GRCh37.p13 chr19: 49,552,685-49,558,265 LOC100287489, CGB8, 1 more genes
    nsv5873865copy number variation1nstd209human GRCh38 chr19: 49,053,790-49,056,034 , GRCh37.p13 chr19: 49,557,047-49,559,291 CGB7
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5590265copy number variation1nstd207human GRCh38 chr19: 49,054,012-49,054,913 , GRCh37.p13 chr19: 49,557,269-49,558,170 CGB7
    nsv5528980copy number variation1nstd206human GRCh38 chr19: 49,048,941-49,055,577 , GRCh37.p13 chr19: 49,552,198-49,558,834 CGB8, CGB7, 1 more genes
    nsv5297960copy number variation1nstd204human GRCh38.p13 chr19: 49,053,890-49,055,633 , GRCh37.p13 chr19: 49,557,147-49,558,890 CGB7
    nsv5292971copy number variation1nstd204human GRCh38.p13 chr19: 49,049,428-49,054,089 , GRCh37.p13 chr19: 49,552,685-49,557,346 LOC100287489, CGB8, 1 more genes
    nsv5292337copy number variation1nstd204human GRCh38.p13 chr19: 49,049,328-49,057,075 , GRCh37.p13 chr19: 49,552,585-49,560,332 LOC100287489, NTF4, 2 more genes
    nsv5020960copy number variation1nstd200human GRCh38 chr19: 49,049,440-49,056,003 , GRCh37.p13 chr19: 49,552,697-49,559,260 LOC100287489, CGB8, 1 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
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4673507copy number variation1nstd186human GRCh37 chr19: 49,552,692-49,559,329 , GRCh38.p12 chr19: 49,049,435-49,056,072 CGB7, CGB8, 1 more genes
    nsv4633085copy number variation1nstd183human GRCh37 chr19: 49,552,692-49,559,329 , GRCh38.p12 chr19: 49,049,435-49,056,072 CGB7, LOC100287489, 1 more genes
    nsv4627588copy number variation2nstd183human GRCh37 chr19: 49,518,848-49,559,939 , GRCh38.p12 chr19: 49,015,591-49,056,682 CGB2, NTF6A, 15 more genes
    nsv4626736copy number variation1nstd183human GRCh37 chr19: 49,519,070-49,561,431 , GRCh38.p12 chr19: 49,015,813-49,058,174 SNAR-G2, RUVBL2, 15 more genes
    nsv4457853copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699 DHDH, GRIN2D, 94 more genes
    nsv4424403copy number variation1nstd174human GRCh37 chr19: 49,526,014-49,559,002 , GRCh38.p12 chr19: 49,022,757-49,055,745 CGB2, NTF6A, 11 more genes
    nsv4422995copy number variation1nstd174human GRCh37 chr19: 49,552,584-49,559,329 , GRCh38.p12 chr19: 49,049,327-49,056,072 LOC100287489, CGB8, 1 more genes
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