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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3881310copy number variation1nstd102humanPathogenic GRCh37 chr2: 46,844,000-46,845,330 , GRCh38 chr2: 46,616,861-46,618,191 CRIPT, PIGF
    nsv4347266copy number variation1nstd102humanPathogenic GRCh37 chr2: 46,844,284-46,844,565 , GRCh38.p12 chr2: 46,617,145-46,617,426 CRIPT, PIGF
    nsv6315248copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 46,844,310-46,845,911 , GRCh38.p12 chr2: 46,617,171-46,618,772 CRIPT, PIGF
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CRIPT, CYP1B1-AS1, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 CRIPT, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 CRIPT, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 CRIPT, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 CRIPT, MTND2P22, 3724 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 CRIPT, SLC35F6, 801 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 CRIPT, RPL7P13, 426 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 CRIPT, ATL2, 465 more genes
    nsv3882842copy number variation1nstd102humanPathogenic GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406 CRIPT, STON1, 303 more genes
    nsv3905626copy number variation1nstd102humanPathogenic GRCh37 chr2: 40,965,422-58,090,956 , GRCh38 chr2: 40,738,282-57,863,821 , NCBI36 chr2: 40,818,926-57,944,460 CRIPT, RNU6-433P, 220 more genes
    nsv3919677inversion1nstd102humanPathogenic GRCh38.p12 chr2: 37,893,967-47,442,383 , GRCh37 chr2: 38,121,110-47,669,522 CRIPT, ASS1P2, 151 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 CRIPT, ACTG2, 1713 more genes
    nsv3891309copy number variation1nstd102humanBenign NCBI36 chr2: 46,654,332-46,813,481 , GRCh37 chr2: 46,800,828-46,959,977 , GRCh38 chr2: 46,573,689-46,732,838 CRIPT, PIGF, 4 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 CRIPT, LOC101927723, 1246 more genes
    nsv3906174copy number variation1nstd102humanLikely benign NCBI36 chr2: 46,672,875-47,568,644 , GRCh38 chr2: 46,592,232-47,488,001 , GRCh37 chr2: 46,819,371-47,715,140 CRIPT, EPCAM, 17 more genes
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 CRIPT, PLEKHH2, 151 more genes
    nsv3897499copy number variation1nstd102humanUncertain significance GRCh37 chr2: 46,642,248-48,430,346 , GRCh38 chr2: 46,415,109-48,203,207 , NCBI36 chr2: 46,495,752-48,283,850 CRIPT, MSH2-OT1, 38 more genes
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