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Items: 1 to 20 of 141

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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
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6757704copy number variation1nstd229human GRCh38 chr4: 99,155,783-99,191,741 , GRCh37.p13 chr4: 100,076,940-100,112,898 PCNAP1, PCNAP2, 1 more genes
    nsv6754642copy number variation1nstd229human GRCh38 chr4: 99,102,725-99,212,334 , GRCh37.p13 chr4: 100,023,876-100,133,491 LOC100507053, ADH6, 3 more genes
    nsv6750890copy number variation1nstd229human GRCh38 chr4: 99,064,601-99,205,500 , GRCh37.p13 chr4: 99,985,752-100,126,657 ADH5, PCNAP1, 4 more genes
    nsv6740025copy number variation1nstd229human GRCh38 chr4: 99,026,449-99,231,369 , GRCh37.p13 chr4: 99,947,600-100,152,526 PCNAP2, ADH6, 5 more genes
    nsv6630192copy number variation1nstd224human GRCh37 chr4: 99,863,585-100,335,586 , GRCh38.p12 chr4: 98,942,434-99,414,429 ADH1B, ADH5, 15 more genes
    nsv6629271copy number variation1nstd224human GRCh37 chr4: 100,042,262-100,131,746 , GRCh38.p12 chr4: 99,121,111-99,210,589 PCNAP1, ADH4, 3 more genes
    nsv6313762copy number variation1nstd102humanUncertain significance GRCh37 chr4: 99,835,828-100,089,147 , GRCh38.p12 chr4: 98,914,677-99,167,990 PCNAP2, RNU7-149P, 10 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6135629copy number variation1nstd213human GRCh37 chr4: 99,690,000-100,180,001 , GRCh38.p12 chr4: 98,768,849-99,258,844 ADH4, ADH5, 13 more genes
    nsv6135624copy number variation1nstd213human GRCh37 chr4: 94,300,000-108,550,001 , GRCh38.p12 chr4: 93,378,849-107,628,845 , ADH1A, 146 more genes
    nsv6135091copy number variation1nstd213human GRCh37 chr4: 94,310,000-108,550,001 , GRCh38.p12 chr4: 93,388,849-107,628,845 , ADH1A, 146 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
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