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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 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
    nsv5455685copy number variation1nstd206human GRCh38 chr4: 114,672,528-114,777,416 , GRCh37.p13 chr4: 115,593,684-115,698,572 CIR1P2, UGT8, 1 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv5030872inversion1nstd200human GRCh38 chr4: 114,129,195-115,314,517 , GRCh37.p13 chr4: 115,050,351-116,235,673 LOC105377380, RN7SL808P, 9 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4808079copy number variation1nstd200human GRCh37 chr4: 115,634,582-115,635,575 , GRCh38.p12 chr4: 114,713,426-114,714,419 CIR1P2
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4455788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 114,579,245-115,640,604 , GRCh38.p12 chr4: 113,658,089-114,719,448 CAMK2D, CIR1P2, 10 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv3920388copy number variation1nstd102humanPathogenic GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207 MIR576, ABT1P1, 447 more genes
    nsv3916316copy number variation1nstd102humanUncertain significance NCBI36 chr4: 111,318,515-191,263,063 , GRCh37.p13 chr4: 111,099,066-191,029,082 , GRCh38.p12 chr4: 110,177,910-190,107,927 RNU7-194P, FOSL1P1, 939 more genes
    nsv3911834copy number variation1nstd102humanLikely pathogenic NCBI36 chr4: 112,210,390-117,832,483 , GRCh37 chr4: 111,990,941-117,613,035 , GRCh38 chr4: 111,069,785-116,691,879 ANK2, CAMK2D, 71 more genes
    nsv3885667copy number variation1nstd102humanUncertain significance GRCh37 chr4: 115,565,977-115,890,735 , GRCh38.p12 chr4: 114,644,821-114,969,579 MIR577, RN7SL808P, 4 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 MTND4LP29, RNU6-128P, 2341 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 LOC105377343, PDGFC, 2341 more genes
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