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Items: 1 to 20 of 51

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895962copy number variation1nstd102humanBenign GRCh37 chr7: 12,339,360-12,430,812 , GRCh38.p12 chr7: 12,299,734-12,391,186 VWDE
    nsv3896134copy number variation1nstd102humanLikely benign GRCh37 chr7: 12,376,699-12,428,489 , GRCh38.p12 chr7: 12,337,073-12,388,863 VWDE
    nsv3883073copy number variation1nstd102humannot provided GRCh38 chr7: 12,378,976-12,383,095 , GRCh37 chr7: 12,418,602-12,422,721 VWDE
    esv3648344copy number variation1estd216humannot provided GRCh37 chr7: 12,418,602-12,422,721 , GRCh38.p12 chr7: 12,378,976-12,383,095 VWDE
    nsv3904837copy number variation1nstd102humanBenign GRCh37 chr7: 12,357,429-12,444,157 , GRCh38.p12 chr7: 12,317,803-12,404,531 VWDE, LOC105375154
    nsv3898276copy number variation1nstd102humanBenign GRCh37 chr7: 12,418,144-12,444,157 , GRCh38.p12 chr7: 12,378,518-12,404,531 VWDE, LOC105375154
    nsv6636793copy number variation1nstd102humanUncertain significance GRCh37 chr7: 12,227,724-12,410,707 , GRCh38.p12 chr7: 12,188,098-12,371,081 VWDE, TMEM106B
    nsv4729005copy number variation1nstd102humanUncertain significance GRCh37 chr7: 12,264,398-12,381,616 , GRCh38.p12 chr7: 12,224,772-12,341,990 VWDE, TMEM106B
    nsv6314302complex chromosomal rearrangement6nstd102humanPathogenic GRCh37 chr3: 149,332,307-149,332,307 , GRCh37 chr3: 154,453,976-154,453,976 , GRCh37 chr3: 149,332,307-149,332,307 , GRCh37 chr3: 154,453,975-154,453,975 , GRCh37 chr7: 12,374,295-12,374,295 , GRCh37 chr7: 12,374,296-12,374,296 , GRCh37 chr10: 28,823,742-28,823,742 , GRCh37 chr10: 11,940,759-11,940,759 , GRCh37 chr10: 102,794,873-102,794,873 , GRCh37 chr10: 102,794,873-102,794,873 , GRCh37 chr10: 11,940,757-11,940,757 , GRCh37 chr10: 28,823,741-28,823,741 , GRCh38.p12 chr10: 101,035,116-101,035,116 , GRCh38.p12 chr10: 28,534,812-28,534,812 , GRCh38.p12 chr10: 11,898,758-11,898,758 , GRCh38.p12 chr10: 101,035,116-101,035,116 , GRCh38.p12 chr10: 11,898,760-11,898,760 , GRCh38.p12 chr10: 28,534,813-28,534,813 , GRCh38.p12 chr3: 149,614,520-149,614,520 , GRCh38.p12 chr3: 149,614,520-149,614,520 , GRCh38.p12 chr3: 154,736,187-154,736,187 , GRCh38.p12 chr3: 154,736,186-154,736,186 , GRCh38.p12 chr7: 12,334,669-12,334,669 , GRCh38.p12 chr7: 12,334,670-12,334,670 VWDE, SFXN3, 2 more genes
    nsv3904356copy number variation1nstd102humanUncertain significance GRCh37 chr7: 12,277,152-12,493,390 , GRCh38.p12 chr7: 12,237,526-12,453,764 VWDE, TMEM106B, 3 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 VWDE, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 VWDE, LOC107986817, 2014 more genes
    nsv3915219copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,649,696-25,800,180 , GRCh38 chr7: 10,610,069-25,760,560 , NCBI36 chr7: 10,616,221-25,766,705 VWDE, SNORD93, 176 more genes
    nsv6313854copy number variation1nstd102humanPathogenic GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463 VWDE, LOC107986766, 115 more genes
    nsv3913922copy number variation1nstd102humanPathogenic GRCh38 chr7: 9,975,653-19,356,878 , NCBI36 chr7: 9,981,805-19,363,026 , GRCh37 chr7: 10,015,280-19,396,501 VWDE, NPM1P13, 86 more genes
    nsv3912345copy number variation1nstd102humanPathogenic NCBI36 chr7: 8,962,614-17,387,487 , GRCh37.p13 chr7: 8,996,089-17,420,962 , GRCh38.p12 chr7: 8,956,459-17,381,338 VWDE, RAD17P1, 78 more genes
    nsv3923125copy number variation1nstd102humanPathogenic GRCh38 chr7: 11,122,492-16,479,303 , NCBI36 chr7: 11,128,644-16,485,453 , GRCh37 chr7: 11,162,119-16,518,928 VWDE, THRAP3P3, 43 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 VWDE, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 VWDE, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 VWDE, MNX1-AS2, 2682 more genes
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