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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053883inversion1nstd229human GRCh38 chr2: 97,357,330-98,588,488 , GRCh37.p13 chr2: 98,087,758-99,204,951 COX5B, ZAP70, 18 more genes
    nsv7049314inversion1nstd229human GRCh38 chr2: 97,164,836-98,594,834 , GRCh37.p13 chr2: 97,830,573-99,211,297 LOC105373501, ATP5F1BP1, 23 more genes
    nsv6696050copy number variation1nstd229human GRCh38 chr2: 98,498,679-98,503,985 , GRCh37.p13 chr2: 99,115,142-99,120,448 INPP4A
    nsv6695379copy number variation1nstd229human GRCh38 chr2: 98,554,901-98,557,100 , GRCh37.p13 chr2: 99,171,364-99,173,563 INPP4A
    nsv6693539copy number variation1nstd229human GRCh38 chr2: 98,398,143-98,572,107 , GRCh37.p13 chr2: 99,014,606-99,188,570 CNGA3, INPP4A
    nsv6693305copy number variation1nstd229human GRCh38 chr2: 98,593,884-98,593,936 , GRCh37.p13 chr2: 99,210,347-99,210,399 INPP4A
    nsv6691832copy number variation1nstd229human GRCh38 chr2: 97,998,382-98,548,364 , GRCh37.p13 chr2: 98,614,845-99,164,827 INPP4A, CNGA3, 3 more genes
    nsv6691657copy number variation1nstd229human GRCh38 chr2: 98,461,278-98,461,695 , GRCh37.p13 chr2: 99,077,741-99,078,158 INPP4A
    nsv6691468copy number variation1nstd229human GRCh38 chr2: 98,536,842-98,539,683 , GRCh37.p13 chr2: 99,153,305-99,156,146 INPP4A
    nsv6687024copy number variation1nstd229human GRCh38 chr2: 98,464,909-98,469,136 , GRCh37.p13 chr2: 99,081,372-99,085,599 INPP4A
    nsv6686540copy number variation1nstd229human GRCh38 chr2: 98,531,846-98,531,938 , GRCh37.p13 chr2: 99,148,309-99,148,401 INPP4A
    nsv6685582copy number variation1nstd229human GRCh38 chr2: 98,494,610-98,501,956 , GRCh37.p13 chr2: 99,111,073-99,118,419 INPP4A
    nsv6685216copy number variation1nstd229human GRCh38 chr2: 98,497,968-98,497,999 , GRCh37.p13 chr2: 99,114,431-99,114,462 INPP4A
    nsv6683918copy number variation1nstd229human GRCh38 chr2: 98,503,031-98,515,752 , GRCh37.p13 chr2: 99,119,494-99,132,215 INPP4A
    nsv6682239copy number variation1nstd229human GRCh38 chr2: 98,463,150-98,468,456 , GRCh37.p13 chr2: 99,079,613-99,084,919 INPP4A
    nsv6679921copy number variation1nstd229human GRCh38 chr2: 98,537,431-98,537,459 , GRCh37.p13 chr2: 99,153,894-99,153,922 INPP4A
    nsv6679120copy number variation1nstd229human GRCh38 chr2: 98,455,771-98,460,434 , GRCh37.p13 chr2: 99,072,234-99,076,897 INPP4A
    nsv6636716copy number variation1nstd102humanUncertain significance GRCh37 chr2: 98,958,721-99,205,212 , GRCh38.p12 chr2: 98,342,258-98,588,749 CNGA3, INPP4A
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
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