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Items: 1 to 20 of 613

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136974copy number variation1nstd102humanUncertain significance GRCh37 chr2: 98,703,594-98,797,478 , GRCh38.p12 chr2: 98,087,131-98,181,015 VWA3B
    nsv7053883inversion1nstd229human GRCh38 chr2: 97,357,330-98,588,488 , GRCh37.p13 chr2: 98,087,758-99,204,951 COX5B, ZAP70, 18 more genes
    nsv7050860inversion1nstd229human GRCh38 chr2: 97,948,396-98,130,122 , GRCh37.p13 chr2: 98,564,859-98,746,585 TMEM131, VWA3B, 1 more genes
    nsv7050653inversion1nstd229human GRCh38 chr2: 98,091,328-98,094,164 , GRCh37.p13 chr2: 98,707,791-98,710,627 VWA3B
    nsv7049314inversion1nstd229human GRCh38 chr2: 97,164,836-98,594,834 , GRCh37.p13 chr2: 97,830,573-99,211,297 LOC105373501, ATP5F1BP1, 23 more genes
    nsv7045794inversion1nstd229human GRCh38 chr2: 98,208,434-98,224,649 , GRCh37.p13 chr2: 98,824,897-98,841,112 VWA3B
    nsv7039903inversion1nstd229human GRCh38 chr2: 98,202,175-98,206,234 , GRCh37.p13 chr2: 98,818,638-98,822,697 ATP5F1BP1, VWA3B
    nsv6697033copy number variation1nstd229human GRCh38 chr2: 98,288,201-98,290,900 , GRCh37.p13 chr2: 98,904,664-98,907,363 VWA3B
    nsv6696896copy number variation1nstd229human GRCh38 chr2: 98,153,145-98,160,534 , GRCh37.p13 chr2: 98,769,608-98,776,997 VWA3B
    nsv6695954copy number variation1nstd229human GRCh38 chr2: 98,226,603-98,226,679 , GRCh37.p13 chr2: 98,843,066-98,843,142 VWA3B
    nsv6695914copy number variation1nstd229human GRCh38 chr2: 98,275,329-98,275,480 , GRCh37.p13 chr2: 98,891,792-98,891,943 VWA3B
    nsv6695221copy number variation1nstd229human GRCh38 chr2: 98,089,203-98,241,850 , GRCh37.p13 chr2: 98,705,666-98,858,313 VWA3B, ATP5F1BP1
    nsv6695134copy number variation1nstd229human GRCh38 chr2: 98,098,076-98,108,087 , GRCh37.p13 chr2: 98,714,539-98,724,550 VWA3B
    nsv6693755copy number variation1nstd229human GRCh38 chr2: 98,197,059-98,205,974 , GRCh37.p13 chr2: 98,813,522-98,822,437 VWA3B, ATP5F1BP1
    nsv6692411copy number variation1nstd229human GRCh38 chr2: 98,306,902-98,307,083 , GRCh37.p13 chr2: 98,923,365-98,923,546 VWA3B
    nsv6692157copy number variation1nstd229human GRCh38 chr2: 98,118,853-98,133,003 , GRCh37.p13 chr2: 98,735,316-98,749,466 VWA3B
    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
    nsv6691632copy number variation1nstd229human GRCh38 chr2: 98,247,196-98,318,073 , GRCh37.p13 chr2: 98,863,659-98,934,536 VWA3B
    nsv6691091copy number variation1nstd229human GRCh38 chr2: 98,152,707-98,155,924 , GRCh37.p13 chr2: 98,769,170-98,772,387 VWA3B
    nsv6689655copy number variation1nstd229human GRCh38 chr2: 98,149,701-98,152,700 , GRCh37.p13 chr2: 98,766,164-98,769,163 VWA3B
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