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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4078727copy number variation1nstd166human GRCh37.p13 chr2: 177,019,044-177,019,116 , GRCh38.p12 chr2: 176,154,316-176,154,388 HOXD4
    esv3022888copy number variation1estd209human GRCh37 chr2: 177,018,791-177,018,792 , GRCh38.p12 chr2: 176,154,063-176,154,064 HOXD4
    nsv6243494mobile element insertion1nstd215human GRCh38 chr2: 176,154,156-176,154,156 , GRCh37.p13 chr2: 177,018,884-177,018,884 HOXD4
    nsv2049457short tandem repeat3nstd128human GRCh37 chr2: 177,018,792-177,018,803 , GRCh38.p12 chr2: 176,154,064-176,154,075 HOXD4
    nsv6690266copy number variation1nstd229human GRCh38 chr2: 176,142,400-176,150,850 , GRCh37.p13 chr2: 177,007,128-177,015,578 HOXD4, MIR10B
    nsv6688237copy number variation1nstd229human GRCh38 chr2: 176,151,462-176,156,437 , GRCh37.p13 chr2: 177,016,190-177,021,165 HOXD4, HOXD3
    nsv6345695copy number variation1nstd223human GRCh38 chr2: 176,151,462-176,156,434 , GRCh37.p13 chr2: 177,016,190-177,021,162 HOXD4, HOXD3
    nsv4078095copy number variation1nstd166human GRCh37.p13 chr2: 177,016,190-177,021,162 , GRCh38.p12 chr2: 176,151,462-176,156,434 HOXD4, HOXD3
    nsv2081658short tandem repeat2nstd128human GRCh37 chr2: 177,015,345-177,015,377 , GRCh38.p12 chr2: 176,150,617-176,150,649 HOXD4, MIR10B
    nsv2049456short tandem repeat1nstd128human GRCh37 chr2: 177,014,798-177,014,827 , GRCh38.p12 chr2: 176,150,070-176,150,099 HOXD4, MIR10B
    nsv2053879short tandem repeat1nstd128human GRCh37 chr2: 177,020,512-177,020,529 , GRCh38.p12 chr2: 176,155,784-176,155,801 HOXD4, HOXD3
    nsv2053878short tandem repeat1nstd128human GRCh37 chr2: 177,014,111-177,014,128 , GRCh38.p12 chr2: 176,149,383-176,149,400 HOXD4, MIR10B
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 HOXD4, DAZAP2P1, 2991 more genes
    nsv3894939copy number variation1nstd102humanPathogenic NCBI36 chr2: 175,471,822-204,514,516 , GRCh37 chr2: 175,763,576-204,806,271 , GRCh38 chr2: 174,898,848-203,941,548 HOXD4, TRE-TTC9-1, 412 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 HOXD4, LINC01117, 339 more genes
    nsv4674757copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858 HOXD4, OSBPL6, 256 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 HOXD4, RBM45, 258 more genes
    nsv3904056copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,821,892-183,059,789 , NCBI36 chr2: 164,530,138-182,768,034 , GRCh38 chr2: 163,965,382-182,195,062 HOXD4, PRKRA, 256 more genes
    nsv3891673copy number variation1nstd102humanPathogenic GRCh37 chr2: 172,285,743-190,044,294 , GRCh38 chr2: 171,429,233-189,179,568 , NCBI36 chr2: 171,993,989-189,752,539 HOXD4, LOC729141, 238 more genes
    nsv3905582copy number variation1nstd102humanPathogenic GRCh38 chr2: 176,086,763-193,201,970 , NCBI36 chr2: 176,659,737-193,774,941 , GRCh37 chr2: 176,951,491-194,066,696 HOXD4, RPL23AP35, 211 more genes
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