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Items: 15

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    Number of Variants: 15

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3115044copy number variation3nstd145human GRCh37 chr16: 55,794,900-55,821,304 , GRCh38.p12 chr16: 55,760,988-55,787,392 CES1P1
    nsv3112538copy number variation1nstd145human GRCh37 chr7: 143,425,305-143,433,546 , GRCh38.p12 chr7: 143,728,212-143,736,453 , GRCh38.p12 chr7|NW_018654714.1: 272,531-280,773 TCAF2
    nsv3116783copy number variation1nstd145human GRCh37 chr7: 110,182,897-110,189,105 , GRCh38.p12 chr7: 110,542,840-110,549,048 LOC105375451
    nsv3116310copy number variation1nstd145human GRCh37 chr16: 6,967,494-6,973,023 , GRCh38.p12 chr16: 6,917,493-6,923,022 RBFOX1
    nsv3116148copy number variation97nstd145human GRCh37 chr8: 594,429-599,002 , GRCh38.p12 chr8: 644,429-649,002 ERICH1
    nsv3110593copy number variation88nstd145human GRCh37 chr8: 40,774,871-40,779,295 , GRCh38.p12 chr8: 40,917,352-40,921,776 LOC105379389
    nsv3112546copy number variation1nstd145human GRCh37 chrX: 32,081,680-32,083,432 , GRCh38.p12 chrX: 32,063,563-32,065,315 DMD
    nsv3117321copy number variation25nstd145human GRCh37 chrX: 69,024,517-69,026,173 , GRCh38.p12 chrX: 69,804,673-69,806,329 EDA
    nsv3117646copy number variation1nstd145human GRCh37 chr5: 32,125,197-32,144,338 , GRCh38.p12 chr5: 32,125,091-32,144,232 GOLPH3
    nsv3117756copy number variation6nstd145human GRCh37 chr1: 248,739,582-248,795,189 , GRCh38.p12 chr1: 248,576,281-248,631,888 OR2T10, OR2T11
    nsv3110686copy number variation2nstd145human GRCh37 chr6: 32,569,983-32,627,343 , GRCh38.p12 chr6: 32,602,206-32,659,566 HLA-DQA1, HLA-DQB1, 2 more genes
    nsv3116118copy number variation124nstd145human GRCh37 chr6: 103,737,578-103,760,261 , GRCh38.p12 chr6: 103,289,703-103,312,386 0
    nsv3111608copy number variation5nstd145human GRCh37 chr5: 140,215,052-140,228,081 , GRCh38.p12 chr5: 140,835,467-140,848,496 PCDHA7, PCDHA1, 8 more genes
    nsv3112313copy number variation7nstd145human GRCh37 chr14: 40,610,218-40,616,291 , GRCh38.p12 chr14: 40,141,014-40,147,087 0
    nsv3114590copy number variation2nstd145human GRCh37 chr4: 112,423,277-112,425,930 , GRCh38.p12 chr4: 111,502,121-111,504,774 0
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