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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887501copy number variation2nstd209human GRCh38 chr19: 49,024,539-49,034,617 , GRCh37.p13 chr19: 49,527,796-49,537,874 CGB3, NTF6A, 4 more genes
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5586054copy number variation1nstd207human GRCh38 chr19: 49,026,793-49,051,540 , GRCh37.p13 chr19: 49,530,050-49,554,797 LOC100287489, NTF6B, 8 more genes
    nsv5518962copy number variation1nstd206human GRCh38 chr19: 49,025,486-49,038,422 , GRCh37.p13 chr19: 49,528,743-49,541,679 NTF6A, NTF6B, 5 more genes
    nsv5020956copy number variation1nstd200human GRCh38 chr19: 49,022,818-49,051,090 , GRCh37.p13 chr19: 49,526,075-49,554,347 CGB8, NTF6A, 10 more genes
    nsv4853302copy number variation1nstd200human GRCh37 chr19: 49,527,762-49,540,820 , GRCh38.p12 chr19: 49,024,505-49,037,563 CGB3, NTF6A, 6 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
    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
    nsv4420611copy number variation1nstd174human GRCh37 chr19: 49,518,848-49,562,658 , GRCh38.p12 chr19: 49,015,591-49,059,401 CGB5, CGB8, 15 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4371559copy number variation1nstd173human GRCh37 chr19: 49,456,001-49,535,375 , GRCh38.p12 chr19: 48,952,744-49,032,118 FTL, RUVBL2, 10 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4272132copy number variation1nstd166human GRCh37.p13 chr19: 49,529,000-49,540,500 , GRCh38.p12 chr19: 49,025,743-49,037,243 NTF6A, NTF6B, 5 more genes
    nsv4268084copy number variation1nstd166human GRCh37.p13 chr19: 49,526,076-49,554,325 , GRCh38.p12 chr19: 49,022,819-49,051,068 NTF6B, LOC100287489, 10 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
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