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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146990insertion1nstd232human GRCh37.p13 chr7: 66,453,486-66,453,486 , GRCh38.p12 chr7: 66,988,499-66,988,499 SBDS
    nsv7099001copy number variation1nstd102humanPathogenic GRCh38 chr7: 66,971,410-66,990,307 , GRCh37 chr7: 66,436,397-66,455,294 RN7SL43P, SBDS
    nsv7098834copy number variation1nstd102humanPathogenic GRCh38 chr7: 66,992,994-66,993,865 , GRCh37 chr7: 66,457,981-66,458,852 SBDS
    nsv7050458inversion1nstd229human GRCh38 chr7: 66,139,390-67,448,632 , GRCh37.p13 chr7: 65,604,377-66,913,619 SAPCD2P3, SPDYE21, 32 more genes
    nsv7041397inversion1nstd229human GRCh38 chr7: 65,600,026-71,276,703 , GRCh37.p13 chr7: 65,286,678-70,741,689 GALNT17, MTCO1P25, 74 more genes
    nsv6836457copy number variation1nstd229human GRCh38 chr7: 66,988,954-66,988,987 , GRCh37.p13 chr7: 66,453,941-66,453,974 SBDS
    nsv6836158copy number variation1nstd229human GRCh38 chr7: 66,987,312-66,990,308 , GRCh37.p13 chr7: 66,452,299-66,455,295 SBDS
    nsv6833841copy number variation1nstd229human GRCh38 chr7: 66,909,245-67,267,085 , GRCh37.p13 chr7: 66,374,232-66,732,072 RN7SL43P, SBDS, 4 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6617096copy number variation1nstd223human GRCh38 chr7: 66,946,768-67,436,672 , GRCh37.p13 chr7: 66,411,755-66,901,659 SBDS, TMEM248, 8 more genes
    nsv6605942copy number variation1nstd223human GRCh38 chr7: 66,983,260-67,003,915 , GRCh37.p13 chr7: 66,448,247-66,468,902 SBDS, TYW1
    nsv6605318copy number variation1nstd223human GRCh38 chr7: 66,969,746-66,986,695 , GRCh37.p13 chr7: 66,434,733-66,451,682 SBDS, RN7SL43P
    nsv6602402copy number variation1nstd223human GRCh38 chr7: 66,947,709-67,075,566 , GRCh37.p13 chr7: 66,412,696-66,540,553 SBDS, TMEM248, 2 more genes
    nsv6571139inversion1nstd223human GRCh38 chr7: 66,977,695-72,844,217 , GRCh37.p13 chr7: 66,442,682-71,935,721 LINC01372, TYW1B, 45 more genes
    nsv6562148inversion1nstd223human GRCh38 chr7: 66,989,250-66,990,301 , GRCh37.p13 chr7: 66,454,237-66,455,288 SBDS
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312786copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 65,556,983-66,460,414 , GRCh38.p12 chr7: 66,091,996-66,995,427 ASL, SKP1P1, 27 more genes
    nsv6291453copy number variation1nstd102humanUncertain significance GRCh38 chr7: 66,791,158-67,272,772 , GRCh37.p13 chr7: 66,256,145-66,737,759 SBDS, GTF2IP23, 9 more genes
    nsv6291337copy number variation1nstd102humanUncertain significance GRCh37 chr7: 66,288,000-66,818,352 , GRCh38.p12 chr7: 66,823,013-67,353,365 RNU6-1254P, LINC01372, 13 more genes
    nsv6135777copy number variation1nstd213human GRCh37 chr7: 65,150,000-70,530,001 , GRCh38.p12 chr7: 65,685,031-71,065,015 ASL, GUSB, 72 more genes
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