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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7142991insertion1nstd232human GRCh37.p13 chr4: 57,834,682-57,834,682 , GRCh38.p12 chr4: 56,968,516-56,968,516 NOA1
    nsv7142428insertion1nstd232human GRCh37.p13 chr4: 57,832,903-57,832,903 , GRCh38.p12 chr4: 56,966,737-56,966,737 NOA1
    nsv7054928inversion1nstd229human GRCh38 chr4: 56,642,680-60,318,047 , GRCh37.p13 chr4: 57,508,846-61,183,765 LOC107986228, POLR2B, 26 more genes
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6733267copy number variation1nstd229human GRCh38 chr4: 56,667,201-57,013,100 , GRCh37.p13 chr4: 57,533,367-57,879,266 SPINK2, CHAER1, 11 more genes
    nsv6729650copy number variation1nstd229human GRCh38 chr4: 56,032,001-57,014,500 , GRCh37.p13 chr4: 56,898,167-57,880,666 REST, RPL7AP31, 27 more genes
    nsv6729057copy number variation1nstd229human GRCh38 chr4: 56,962,771-56,971,292 , GRCh37.p13 chr4: 57,828,937-57,837,458 NOA1
    nsv6725938copy number variation1nstd229human GRCh38 chr4: 56,972,200-56,975,943 , GRCh37.p13 chr4: 57,838,366-57,842,109 NOA1
    nsv6723082copy number variation1nstd229human GRCh38 chr4: 56,763,701-56,963,400 , GRCh37.p13 chr4: 57,629,867-57,829,566 REST, RN7SL357P, 4 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6575116inversion1nstd223human GRCh38 chr4: 56,642,680-60,318,047 , GRCh37.p13 chr4: 57,508,846-61,183,765 LOC105377666, RN7SL357P, 26 more genes
    nsv6390914copy number variation1nstd223human GRCh38 chr4: 56,972,201-56,976,000 , GRCh37.p13 chr4: 57,838,367-57,842,166 NOA1
    nsv6388921copy number variation1nstd223human GRCh38 chr4: 56,963,186-56,967,167 , GRCh37.p13 chr4: 57,829,352-57,833,333 NOA1
    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
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv6135592copy number variation1nstd213human GRCh37 chr4: 57,660,000-57,980,001 , GRCh38.p12 chr4: 56,793,834-57,113,835 IGFBP7, POLR2B, 9 more genes
    nsv6135345copy number variation1nstd213human GRCh37 chr4: 55,360,000-63,180,001 , GRCh38.p12 chr4: 54,493,833-62,314,283 GLDCP1, IGFBP7, 82 more genes
    nsv6134939copy number variation1nstd213human GRCh37 chr4: 55,330,000-63,180,001 , GRCh38.p12 chr4: 54,463,833-62,314,283 GLDCP1, IGFBP7, 82 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
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