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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904337copy number variation1nstd209human GRCh38 chr3: 112,990,056-112,991,184 , GRCh37.p13 chr3: 112,708,903-112,710,031 GTPBP8
    nsv5833945copy number variation1nstd209human GRCh38 chr3: 112,990,011-112,991,210 , GRCh37.p13 chr3: 112,708,858-112,710,057 GTPBP8
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4728380copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,135,341-115,509,260 , GRCh38.p12 chr3: 112,416,494-115,790,413 SLC35A5, EIF4E2P2, 51 more genes
    nsv4595964copy number variation1nstd183human GRCh37 chr3: 112,710,165-112,710,837 , GRCh38.p12 chr3: 112,991,318-112,991,990 GTPBP8
    nsv4595961copy number variation1nstd183human GRCh37 chr3: 111,977,032-113,013,191 , GRCh38.p12 chr3: 112,258,185-113,294,344 , NEPRO-AS1, 22 more genes
    nsv4584893copy number variation1nstd183human GRCh37 chr3: 112,701,827-112,714,022 , GRCh38.p12 chr3: 112,982,980-112,995,175 GTPBP8
    nsv4578248copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,183,943-115,492,949 , GRCh38.p12 chr3: 112,465,096-115,774,102 ZBTB20, ZBTB20-AS1, 51 more genes
    nsv4452572copy number variation2nstd102humanUncertain significance GRCh37 chr3: 111,929,014-112,773,945 , GRCh38.p12 chr3: 112,210,167-113,055,098 MIR9900, CD200, 16 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv3961744copy number variation1nstd168human GRCh38 chr3: 112,982,085-113,061,954 , GRCh37.p13 chr3: 112,700,932-112,780,801 , NEPRO, 2 more genes
    nsv3924149copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,666,631-116,975,648 , GRCh38 chr3: 112,465,094-115,774,111 , GRCh37 chr3: 112,183,941-115,492,958 ATOSBP1, ZBTB20-AS1, 51 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3922321copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,681,019-116,975,639 , GRCh38 chr3: 112,479,482-115,774,102 , GRCh37 chr3: 112,198,329-115,492,949 NAA50, ATOSBP1, 51 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 QTRT2, MIR544B, 284 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
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