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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 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
    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
    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
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4268551copy number variation1nstd166human GRCh37.p13 chr19: 49,563,787-49,579,456 , GRCh38.p12 chr19: 49,060,530-49,076,199 NTF4, KCNA7
    nsv4262872copy number variation1nstd166human GRCh37.p13 chr19: 49,568,816-49,569,498 , GRCh38.p12 chr19: 49,065,559-49,066,241 NTF4, KCNA7
    nsv3970985insertion1nstd168human GRCh38 chr19: 49,056,485-49,061,818 , GRCh37.p13 chr19: 49,559,742-49,565,075 NTF4, CGB7
    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
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 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
    nsv3895098copy number variation1nstd102humanBenign GRCh37 chr19: 49,556,215-49,651,042 , GRCh38.p12 chr19: 49,052,958-49,147,785 KCNA7, NTF4, 6 more genes
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