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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925901copy number variation1nstd209human GRCh38 chr11: 118,142,733-118,142,825 , GRCh37.p13 chr11: 118,013,448-118,013,540 SCN4B
    nsv5915591copy number variation1nstd209human GRCh38 chr11: 118,076,122-118,161,777 , GRCh37.p13 chr11: 117,946,837-118,032,492 SCN2B, SMIM35, 3 more genes
    nsv5502535copy number variation1nstd206human GRCh38 chr11: 118,139,470-118,144,865 , GRCh37.p13 chr11: 118,010,185-118,015,580 SCN4B
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4989347copy number variation1nstd200human GRCh38 chr11: 118,076,122-118,161,781 , GRCh37.p13 chr11: 117,946,837-118,032,496 SMIM35, SCN4B, 3 more genes
    nsv4980910copy number variation1nstd200human GRCh38 chr11: 118,139,470-118,144,865 , GRCh37.p13 chr11: 118,010,185-118,015,580 SCN4B
    nsv4980909copy number variation1nstd200human GRCh38 chr11: 118,135,633-118,140,106 , GRCh37.p13 chr11: 118,006,348-118,010,821 SCN4B
    nsv4844492copy number variation1nstd200human GRCh37 chr11: 118,010,185-118,015,580 , GRCh38.p12 chr11: 118,139,470-118,144,865 SCN4B
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4683551copy number variation9nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 117,856,768-118,972,385 , GRCh38.p12 chr11: 117,986,053-119,101,675 MIR6716, TREHP1, 48 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
    nsv4451218copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,007,722-119,170,511 , GRCh38.p12 chr11: 118,137,007-119,299,801 ABCG4, CCDC153, 52 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4205845copy number variation1nstd166human GRCh37.p13 chr11: 118,009,627-118,014,939 , GRCh38.p12 chr11: 118,138,912-118,144,224 SCN4B
    nsv4203894copy number variation1nstd166human GRCh37.p13 chr11: 118,010,185-118,015,580 , GRCh38.p12 chr11: 118,139,470-118,144,865 SCN4B
    nsv4203639copy number variation1nstd166human GRCh37.p13 chr11: 117,946,773-118,032,496 , GRCh38.p12 chr11: 118,076,058-118,161,781 TMPRSS4, SCN4B, 3 more genes
    nsv3967128copy number variation1nstd168human GRCh38 chr11: 118,143,675-118,155,940 , GRCh37.p13 chr11: 118,014,390-118,026,655 SCN4B
    nsv3923375copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526 VPS26B, LOC105369531, 390 more genes
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