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Items: 1 to 20 of 3935

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143133copy number variation1nstd232human GRCh37.p13 chr2: 51,222,125-51,222,192 , GRCh38.p12 chr2: 50,994,987-50,995,054 NRXN1
    nsv7137055copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 50,984,755-51,256,334 , GRCh38.p12 chr2: 50,757,617-51,029,196 NRXN1
    nsv7136998copy number variation1nstd102humanPathogenic GRCh37 chr2: 50,214,717-50,293,739 , GRCh38.p12 chr2: 49,987,579-50,066,601 NRXN1
    nsv7136975copy number variation1nstd102humanPathogenic GRCh37 chr2: 51,008,023-51,294,599 , GRCh38.p12 chr2: 50,780,885-51,067,461 NRXN1, NRXN1-DT
    nsv7096891copy number variation1nstd102humanUncertain significance GRCh37 chr2: 50,779,705-50,850,773 , GRCh38.p12 chr2: 50,552,567-50,623,635 MTCO1P42, NRXN1, 1 more genes
    nsv7096890copy number variation1nstd102humanUncertain significance GRCh37 chr2: 50,765,371-50,850,773 , GRCh38.p12 chr2: 50,538,233-50,623,635 MTCO1P42, NRXN1, 1 more genes
    nsv7096889copy number variation1nstd102humanPathogenic GRCh37 chr2: 50,463,907-51,255,411 , GRCh38.p12 chr2: 50,236,769-51,028,273 MIR8485, NRXN1, 2 more genes
    nsv7096668copy number variation1nstd102humanPathogenic GRCh37 chr2: 51,153,056-51,255,411 , GRCh38.p12 chr2: 50,925,918-51,028,273 NRXN1
    nsv7096667copy number variation1nstd102humanUncertain significance GRCh37 chr2: 50,847,140-50,848,407 , GRCh38.p12 chr2: 50,620,002-50,621,269 LOC101927089, NRXN1
    nsv7096514copy number variation1nstd102humanUncertain significance GRCh37 chr2: 48,914,836-50,850,773 , GRCh38.p12 chr2: 48,687,697-50,623,635 STON1-GTF2A1L, LOC105374594, 12 more genes
    nsv7096175copy number variation1nstd102humanPathogenic GRCh37 chr2: 51,254,620-51,255,411 , GRCh38.p12 chr2: 51,027,482-51,028,273 NRXN1
    nsv7096174copy number variation1nstd102humanUncertain significance GRCh37 chr2: 51,148,987-51,149,845 , GRCh38.p12 chr2: 50,921,849-50,922,707 NRXN1
    nsv7096173copy number variation1nstd102humanPathogenic GRCh37 chr2: 50,723,023-50,780,183 , GRCh38.p12 chr2: 50,495,885-50,553,045 NRXN1
    nsv7057224inversion1nstd229human GRCh38 chr2: 50,429,229-50,432,708 , GRCh37.p13 chr2: 50,656,367-50,659,846 NRXN1
    nsv7056979inversion1nstd229human GRCh38 chr2: 50,669,358-50,669,384 , GRCh37.p13 chr2: 50,896,496-50,896,522 NRXN1
    nsv7056111inversion1nstd229human GRCh38 chr2: 48,697,143-51,252,169 , GRCh37.p13 chr2: 48,924,282-51,479,307 CTBP2P5, RPL7P13, 14 more genes
    nsv7055659inversion1nstd229human GRCh38 chr2: 50,993,005-50,993,055 , GRCh37.p13 chr2: 51,220,143-51,220,193 NRXN1
    nsv7055093inversion1nstd229human GRCh38 chr2: 50,628,669-50,633,660 , GRCh37.p13 chr2: 50,855,807-50,860,798 NRXN1, LOC101927089
    nsv7054455inversion1nstd229human GRCh38 chr2: 49,984,602-49,986,624 , GRCh37.p13 chr2: 50,211,740-50,213,762 NRXN1
    nsv7053548inversion1nstd229human GRCh38 chr2: 50,420,374-50,425,449 , GRCh37.p13 chr2: 50,647,512-50,652,587 NRXN1
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