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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7057243inversion1nstd229human GRCh38 chr4: 94,329,030-94,332,331 , GRCh37.p13 chr4: 95,250,181-95,253,482 HPGDS
    nsv7054208inversion1nstd229human GRCh38 chr4: 91,987,159-94,765,936 , GRCh37.p13 chr4: 92,908,310-95,687,087 SMARCAD1-DT, BMPR1B-DT, 14 more genes
    nsv7048783inversion1nstd229human GRCh38 chr4: 94,326,850-94,327,448 , GRCh37.p13 chr4: 95,248,001-95,248,599 HPGDS
    nsv7047278inversion1nstd229human GRCh38 chr4: 92,017,603-94,765,933 , GRCh37.p13 chr4: 92,938,754-95,687,084 ATOH1, LNCPRESS2, 14 more genes
    nsv6755291copy number variation1nstd229human GRCh38 chr4: 91,791,218-94,840,947 , GRCh37.p13 chr4: 92,712,369-95,762,098 HMGB3P15, RPL35AP11, 15 more genes
    nsv6753448copy number variation1nstd229human GRCh38 chr4: 94,318,501-94,323,300 , GRCh37.p13 chr4: 95,239,652-95,244,451 HPGDS
    nsv6753120copy number variation1nstd229human GRCh38 chr4: 94,016,966-94,422,680 , GRCh37.p13 chr4: 94,938,117-95,343,831 SMARCAD1, HMGB3P15, 3 more genes
    nsv6750292copy number variation1nstd229human GRCh38 chr4: 94,065,373-94,822,571 , GRCh37.p13 chr4: 94,986,524-95,743,722 HPGDS, BMPR1B-DT, 6 more genes
    nsv6748880copy number variation1nstd229human GRCh38 chr4: 92,755,485-94,331,886 , GRCh37.p13 chr4: 93,676,636-95,253,037 RACK1P3, SMARCAD1, 6 more genes
    nsv6744442copy number variation1nstd229human GRCh38 chr4: 94,311,201-94,311,900 , GRCh37.p13 chr4: 95,232,352-95,233,051 HPGDS
    nsv6741164copy number variation1nstd229human GRCh38 chr4: 94,318,301-94,338,600 , GRCh37.p13 chr4: 95,239,452-95,259,751 HPGDS
    nsv6739849copy number variation1nstd229human GRCh38 chr4: 94,341,814-94,348,009 , GRCh37.p13 chr4: 95,262,965-95,269,160 HPGDS
    nsv6738718copy number variation1nstd229human GRCh38 chr4: 94,334,643-94,337,061 , GRCh37.p13 chr4: 95,255,794-95,258,212 HPGDS
    nsv6573412inversion1nstd223human GRCh38 chr4: 94,326,850-94,327,448 , GRCh37.p13 chr4: 95,248,001-95,248,599 HPGDS
    nsv6566341inversion1nstd223human GRCh38 chr4: 94,337,040-94,337,352 , GRCh37.p13 chr4: 95,258,191-95,258,503 HPGDS
    nsv6393535copy number variation1nstd223human GRCh38 chr4: 94,319,885-94,576,968 , GRCh37.p13 chr4: 95,241,036-95,498,119 HPGDS, PDLIM5, 1 more genes
    nsv6393378copy number variation1nstd223human GRCh38 chr4: 94,303,947-94,304,317 , GRCh37.p13 chr4: 95,225,098-95,225,468 HPGDS
    nsv6391796copy number variation1nstd223human GRCh38 chr4: 94,311,875-94,322,653 , GRCh37.p13 chr4: 95,233,026-95,243,804 HPGDS
    nsv6389656copy number variation1nstd223human GRCh38 chr4: 94,306,871-94,309,611 , GRCh37.p13 chr4: 95,228,022-95,230,762 HPGDS
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