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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915362copy number variation1nstd209human GRCh38 chr7: 122,122,508-122,182,102 , GRCh37.p13 chr7: 121,762,562-121,822,156 AASS, LOC100130618
    nsv5909902copy number variation1nstd209human GRCh38 chr7: 122,073,928-122,074,102 , GRCh37.p13 chr7: 121,713,982-121,714,156 AASS
    nsv5860477copy number variation1nstd209human GRCh38 chr7: 122,122,916-122,181,853 , GRCh37.p13 chr7: 121,762,970-121,821,907 AASS, LOC100130618
    nsv5691937mobile element insertion2nstd211human GRCh38 chr7: 122,100,308-122,100,308 , GRCh37.p13 chr7: 121,740,362-121,740,362 AASS
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5492093copy number variation1nstd206human GRCh38 chr7: 122,101,760-122,101,825 , GRCh37.p13 chr7: 121,741,814-121,741,879 AASS
    nsv5491546copy number variation1nstd206human GRCh38 chr7: 122,139,302-122,146,879 , GRCh37.p13 chr7: 121,779,356-121,786,933 AASS
    nsv5486617copy number variation1nstd206human GRCh38 chr7: 122,130,935-122,131,049 , GRCh37.p13 chr7: 121,770,989-121,771,103 AASS
    nsv5483345copy number variation1nstd206human GRCh38 chr7: 122,126,773-122,136,287 , GRCh37.p13 chr7: 121,766,827-121,776,341 AASS
    nsv5476487copy number variation1nstd206human GRCh38 chr7: 122,109,920-122,110,335 , GRCh37.p13 chr7: 121,749,974-121,750,389 AASS
    nsv5395166mobile element insertion1nstd206human GRCh38 chr7: 122,100,308-122,100,359 , GRCh37.p13 chr7: 121,740,362-121,740,413 AASS
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5371127translocation1nstd200human GRCh38 chr7: 122,131,049-122,131,049 , GRCh38 chr7: 122,130,935-122,130,935 , GRCh37.p13 chr7: 121,770,989-121,770,989 , GRCh37.p13 chr7: 121,771,103-121,771,103 AASS
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5110285mobile element insertion1nstd203human GRCh38 chr7: 122,141,658-122,141,701 , GRCh37.p13 chr7: 121,781,712-121,781,755 AASS
    nsv5106631mobile element insertion1nstd203human GRCh38 chr7: 122,099,167-122,099,181 , GRCh37.p13 chr7: 121,739,221-121,739,235 AASS
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4958004copy number variation1nstd200human GRCh38 chr7: 122,142,395-122,143,686 , GRCh37.p13 chr7: 121,782,449-121,783,740 AASS
    nsv4958003copy number variation1nstd200human GRCh38 chr7: 122,139,302-122,146,879 , GRCh37.p13 chr7: 121,779,356-121,786,933 AASS
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