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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093699copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,747,968-103,535,657 , GRCh38.p12 chr10: 100,988,211-101,775,900 RNY5P7, TLX1, 25 more genes
    nsv7075098inversion1nstd229human GRCh38 chr10: 101,035,832-101,039,322 , GRCh37.p13 chr10: 102,795,589-102,799,079 SFXN3
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6896298copy number variation1nstd229human GRCh38 chr10: 100,883,101-101,090,000 , GRCh37.p13 chr10: 102,642,858-102,849,757 MIR608, LOC107984262, 9 more genes
    nsv6885171copy number variation1nstd229human GRCh38 chr10: 101,023,532-101,227,683 , GRCh37.p13 chr10: 102,783,289-102,987,440 LOC107984262, LINC01514, 9 more genes
    nsv6882475copy number variation1nstd229human GRCh38 chr10: 101,025,215-101,029,773 , GRCh37.p13 chr10: 102,784,972-102,789,530 SFXN3, PDZD7
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    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 SFXN3, VWDE, 2 more genes
    nsv6308666mobile element insertion1nstd186human GRCh37 chr10: 102,794,337-102,794,388 , GRCh38.p12 chr10: 101,034,580-101,034,631 SFXN3
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv5726042mobile element insertion2nstd211human GRCh38 chr10: 101,034,580-101,034,580 , GRCh37.p13 chr10: 102,794,337-102,794,337 SFXN3
    nsv5559620mobile element insertion1nstd206human GRCh38 chr10: 101,034,580-101,034,631 , GRCh37.p13 chr10: 102,794,337-102,794,388 SFXN3
    nsv5487283copy number variation1nstd206human GRCh38 chr10: 101,031,632-101,032,511 , GRCh37.p13 chr10: 102,791,389-102,792,268 SFXN3, PDZD7
    nsv5320376copy number variation1nstd204human GRCh38.p13 chr10: 101,019,383-101,764,485 , GRCh37.p13 chr10: 102,779,140-103,524,242 , KAZALD1, 23 more genes
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