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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099297copy number variation1nstd231human GRCh38.p12 chr1: 58,444,770-67,143,664 , GRCh37 chr1: 58,910,442-67,609,347 AK4, CYP2J2, 125 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ALG6, MIR3116-2, 94 more genes
    nsv7095538copy number variation1nstd102humanPathogenic GRCh37 chr1: 65,299,551-67,861,772 , GRCh38.p12 chr1: 64,833,868-67,396,089 MRPS21P1, MIER1, 36 more genes
    nsv7055498inversion1nstd229human GRCh38 chr1: 66,514,766-73,182,042 , GRCh37.p13 chr1: 66,980,449-73,647,725 LINC02796, LOC105378789, 80 more genes
    nsv7054976inversion1nstd229human GRCh38 chr1: 66,778,824-69,400,485 , GRCh37.p13 chr1: 67,244,507-69,866,168 ELOCP18, MIR1262, 40 more genes
    nsv6652718copy number variation1nstd229human GRCh38 chr1: 66,792,266-66,798,329 , GRCh37.p13 chr1: 67,257,949-67,264,012 INSL5
    nsv6636512copy number variation1nstd102humanUncertain significance GRCh37 chr1: 66,815,031-67,319,280 , GRCh38.p12 chr1: 66,349,348-66,853,597 DNAI4, LOC105378776, 5 more genes
    nsv6542115inversion1nstd223human GRCh38 chr1: 61,925,268-71,371,290 , GRCh37.p13 chr1: 62,390,940-71,836,973 PATJ, GNG12-AS1, 142 more genes
    nsv6330049copy number variation1nstd223human GRCh38 chr1: 66,792,266-66,798,322 , GRCh37.p13 chr1: 67,257,949-67,264,005 INSL5
    nsv6313537copy number variation1nstd102humanUncertain significance GRCh37 chr1: 65,125,111-69,186,543 , GRCh38.p12 chr1: 64,659,428-68,720,860 RPE65, DNAJB6P4, 64 more genes
    nsv4896096copy number variation1nstd200human GRCh38 chr1: 66,792,266-66,798,322 , GRCh37.p13 chr1: 67,257,949-67,264,005 INSL5
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783563copy number variation1nstd200human GRCh37 chr1: 67,257,949-67,264,005 , GRCh38.p12 chr1: 66,792,266-66,798,322 INSL5
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4453663copy number variation1nstd102humanPathogenic GRCh37 chr1: 59,922,631-72,058,653 , GRCh38.p12 chr1: 59,456,959-71,592,970 RNU6-387P, MIR3671, 170 more genes
    nsv4450384copy number variation1nstd102humannot provided GRCh37 chr1: 66,085,524-88,429,789 , GRCh38.p12 chr1: 65,619,841-87,964,106 DEPDC1, ERICH3-AS1, 264 more genes
    nsv4449847copy number variation1nstd102humanPathogenic GRCh37 chr1: 66,868,168-77,106,425 , GRCh38.p12 chr1: 66,402,485-76,640,740 GNG12-AS1, C1orf141, 118 more genes
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