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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097388copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,530,028-79,082,636 , GRCh38.p12 chr7: 77,900,711-79,453,320 MAGI2-AS3, LOC100421387, 9 more genes
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv6836367copy number variation1nstd229human GRCh38 chr7: 79,013,822-79,771,040 , GRCh37.p13 chr7: 78,643,138-79,400,356 MAGI2-AS3, LOC100421387, 9 more genes
    nsv6835593copy number variation1nstd229human GRCh38 chr7: 79,462,525-79,467,659 , GRCh37.p13 chr7: 79,091,841-79,096,975 MAGI2-AS3
    nsv6829376copy number variation1nstd229human GRCh38 chr7: 79,466,401-79,470,900 , GRCh37.p13 chr7: 79,095,717-79,100,216 MAGI2-AS3
    nsv6818961copy number variation1nstd229human GRCh38 chr7: 79,455,271-79,460,491 , GRCh37.p13 chr7: 79,084,587-79,089,807 MAGI2-AS3
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6618731copy number variation1nstd223human GRCh38 chr7: 78,760,587-79,463,170 , GRCh37.p13 chr7: 78,389,903-79,092,486 MAGI2-AS3, RNU6-337P, 5 more genes
    nsv6610921copy number variation1nstd223human GRCh38 chr7: 79,457,359-79,457,548 , GRCh37.p13 chr7: 79,086,675-79,086,864 MAGI2-AS3
    nsv6610882copy number variation1nstd223human GRCh38 chr7: 79,464,209-79,464,719 , GRCh37.p13 chr7: 79,093,525-79,094,035 MAGI2-AS3
    nsv6606936copy number variation1nstd223human GRCh38 chr7: 79,445,949-79,457,874 , GRCh37.p13 chr7: 79,075,265-79,087,190 MAGI2-AS3, MAGI2
    nsv6603452copy number variation1nstd223human GRCh38 chr7: 79,463,338-79,466,443 , GRCh37.p13 chr7: 79,092,654-79,095,759 MAGI2-AS3
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313880copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,310,644-84,461,089 , GRCh38.p12 chr7: 77,681,327-84,831,773 RNU6-337P, LINC03017, 54 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6313707copy number variation1nstd102humanUncertain significance GRCh37 chr7: 78,430,626-82,605,557 , GRCh38.p12 chr7: 78,801,310-82,976,241 LOC105375369, MAGI2, 37 more genes
    nsv6292911mobile element insertion1nstd186human GRCh37 chr7: 79,094,834-79,094,885 , GRCh38.p12 chr7: 79,465,518-79,465,569 MAGI2-AS3
    nsv6167898copy number variation1nstd214human GRCh38 chr7: 79,468,045-79,468,095 , GRCh37.p13 chr7: 79,097,361-79,097,411 MAGI2-AS3
    nsv6136262copy number variation1nstd213human GRCh37 chr7: 77,010,000-90,950,001 , GRCh38.p12 chr7: 77,380,683-91,320,686 , GRM3, 118 more genes
    nsv6136205copy number variation1nstd213human GRCh37 chr7: 79,050,000-81,680,001 , GRCh38.p12 chr7: 79,420,684-82,050,685 LOC100128317, LOC100420647, 28 more genes
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