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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 PHOSPHO2, DAZAP2P1, 2991 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 PHOSPHO2, LINC01117, 339 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 PHOSPHO2, 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 PHOSPHO2, PRKRA, 256 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 PHOSPHO2, 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 PHOSPHO2, 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 PHOSPHO2, 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 PHOSPHO2, LOC105373739, 95 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 PHOSPHO2, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 PHOSPHO2, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 PHOSPHO2, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 PHOSPHO2, MTND2P22, 3724 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 PHOSPHO2, SNORA41, 663 more genes
    nsv3876037copy number variation1nstd102humanPathogenic GRCh37 chr2: 169,829,974-215,521,436 , GRCh38.p12 chr2: 168,973,464-214,656,712 PHOSPHO2, LINC01953, 632 more genes
    nsv3875392copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,409,978-179,325,736 , GRCh38.p12 chr2: 151,553,464-178,461,009 PHOSPHO2, MIR10B, 359 more genes
    nsv3874278copy number variation1nstd102humanPathogenic GRCh37 chr2: 156,489,430-182,921,298 , GRCh38.p12 chr2: 155,632,918-182,056,571 PHOSPHO2, LOC107985957, 358 more genes
    nsv3893853copy number variation1nstd102humanPathogenic GRCh38 chr2: 154,294,042-175,989,372 , GRCh37 chr2: 155,150,555-176,854,100 , NCBI36 chr2: 154,858,801-176,562,346 PHOSPHO2, SCN7A, 275 more genes
    nsv1398397copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 167,996,718-170,671,886 , GRCh38.p12 chr2: 167,140,208-169,815,376 PHOSPHO2, LRP2, 36 more genes
    nsv3880118copy number variation1nstd102humanBenign GRCh37 chr2: 170,343,083-170,680,879 , GRCh38.p12 chr2: 169,486,573-169,824,369 PHOSPHO2, CYB5AP2, 13 more genes
    nsv3923963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331 PHOSPHO2, NMTRQ-TTG9-1, 1944 more genes
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