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Items: 1 to 20 of 28

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673389copy number variation1nstd102humanPathogenic GRCh37 chr19: 36,317,274-36,326,673 , GRCh38.p12 chr19: 35,826,372-35,835,771 NPHS1
    nsv6310477copy number variation1nstd102humanPathogenic GRCh37 chr19: 36,330,129-36,335,371 , GRCh38.p12 chr19: 35,839,227-35,844,469 NPHS1
    nsv7095276copy number variation1nstd102humanPathogenic GRCh37 chr19: 36,338,828-36,339,610 , GRCh38.p12 chr19: 35,847,926-35,848,708 NPHS1
    nsv4682148copy number variation1nstd102humanPathogenic GRCh37 chr19: 36,326,597-36,326,673 , GRCh38.p12 chr19: 35,835,695-35,835,771 NPHS1
    nsv6314387insertion1nstd102humanPathogenic GRCh37 chr19: 36,336,291-36,336,291 , GRCh38 chr19: 35,845,389-35,845,389 NPHS1
    nsv4682793copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,314,901-36,329,450 , GRCh38.p12 chr19: 35,823,999-35,838,548 NPHS1
    nsv7099006copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,322,665-36,330,138 , GRCh38.p12 chr19: 35,831,763-35,839,236 NPHS1
    nsv7098965copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,337,097-36,340,451 , GRCh38.p12 chr19: 35,846,195-35,849,549 NPHS1
    nsv6310631copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,330,129-36,330,519 , GRCh38.p12 chr19: 35,839,227-35,839,617 NPHS1
    nsv6310630copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,317,416-36,317,567 , GRCh38.p12 chr19: 35,826,514-35,826,665 NPHS1
    nsv7148228copy number variation1nstd102humanPathogenic GRCh38 chr19: 35,811,865-35,846,292 , GRCh37.p13 chr19: 36,302,767-36,337,194 NPHS1, PRODH2
    nsv7093062copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 36,337,097-36,341,265 , GRCh38.p12 chr19: 35,846,195-35,850,363 NPHS1, KIRREL2
    nsv3890831copy number variation1nstd102humanLikely benign GRCh37 chr19: 36,313,074-36,349,382 , GRCh38.p12 chr19: 35,822,172-35,858,480 NPHS1, KIRREL2
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 NPHS1, UBA2, 241 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 NPHS1, MAG, 238 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 NPHS1, ATP4A, 129 more genes
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 NPHS1, SCN1B, 76 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 NPHS1, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 NPHS1, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 NPHS1, LENG8, 2408 more genes
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