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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885189copy number variation1nstd102humanBenign GRCh37 chr2: 170,413,751-170,487,425 , GRCh38.p12 chr2: 169,557,241-169,630,915 PPIG, FASTKD1
    nsv3889975copy number variation1nstd102humanBenign GRCh37 chr2: 170,411,693-170,469,839 , GRCh38.p12 chr2: 169,555,183-169,613,329 PPIG, FASTKD1
    nsv3889593copy number variation1nstd102humanBenign GRCh37 chr2: 170,413,751-170,465,182 , GRCh38.p12 chr2: 169,557,241-169,608,672 PPIG, FASTKD1
    nsv3877822copy number variation1nstd102humanBenign GRCh37 chr2: 170,368,695-170,517,503 , GRCh38.p12 chr2: 169,512,185-169,660,993 PPIG, FASTKD1, 3 more genes
    nsv3888343copy number variation1nstd102humanBenign GRCh37 chr2: 170,344,060-170,469,839 , GRCh38.p12 chr2: 169,487,550-169,613,329 PPIG, BBS5, 2 more genes
    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 PPIG, DAZAP2P1, 2991 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 PPIG, LINC01117, 339 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 PPIG, 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 PPIG, PRKRA, 256 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 PPIG, EIF3EP3, 158 more genes
    nsv3909452copy number variation1nstd102humanPathogenic GRCh37 chr2: 165,706,627-176,423,918 , GRCh38 chr2: 164,850,117-175,559,190 , NCBI36 chr2: 165,414,873-176,132,164 PPIG, LOC107985959, 141 more genes
    nsv3914220copy number variation1nstd102humanPathogenic NCBI36 chr2: 166,992,294-175,094,656 , GRCh37.p13 chr2: 167,284,048-175,386,410 , GRCh38.p12 chr2: 166,427,538-174,521,682 PPIG, GPR155-DT, 111 more genes
    nsv3903934copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,922,548-172,962,614 , NCBI36 chr2: 164,630,794-172,670,860 , GRCh38 chr2: 164,066,038-172,097,886 PPIG, LOC105373739, 95 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 PPIG, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 PPIG, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 PPIG, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 PPIG, MTND2P22, 3724 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 PPIG, SNORA41, 663 more genes
    nsv3876037copy number variation1nstd102humanPathogenic GRCh37 chr2: 169,829,974-215,521,436 , GRCh38.p12 chr2: 168,973,464-214,656,712 PPIG, LINC01953, 632 more genes
    nsv3875392copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,409,978-179,325,736 , GRCh38.p12 chr2: 151,553,464-178,461,009 PPIG, MIR10B, 359 more genes
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