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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 LOC93463, DUSP28, 151 more genes
    nsv4674620copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,265,271-242,783,384 , GRCh38.p12 chr2: 236,356,628-241,841,232 OR6B2, COPS8, 122 more genes
    nsv4674036copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,172,348-241,611,309 , GRCh38.p12 chr2: 235,263,704-240,671,892 ILKAP, MLPH, 95 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv4386900copy number variation1nstd173human GRCh37 chr2: 237,508,557-242,783,396 , GRCh38.p12 chr2: 236,599,914-241,841,244 , LRRFIP1, 123 more genes
    nsv4347297copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,071,623-243,048,760 , GRCh38.p12 chr2: 238,162,982-242,106,609 ANO7, LINC02610, 97 more genes
    nsv4347296copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 238,795,602-242,918,203 , GRCh38.p12 chr2: 237,886,960-241,976,052 AGXT, KIF1A, 101 more genes
    nsv4347295copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,028,693-242,708,080 , GRCh38.p12 chr2: 236,120,049-241,768,665 RBM44, LOC105373947, 123 more genes
    nsv3968640insertion1nstd168human GRCh38 chr2: 238,838,884-238,889,544 , GRCh37.p13 chr2: 239,747,525-239,798,185 TWIST2, LOC100287387
    nsv3924199copy number variation1nstd102humanUncertain significance NCBI36 chr2: 130,861,065-242,751,149 , GRCh37.p13 chr2: 131,144,595-243,102,476 , GRCh38.p12 chr2: 130,387,022-242,160,331 METAP1D, UBE2E3-DT, 1635 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 NMTRQ-TTG9-1, MIR6810, 1944 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 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3910501copy number variation1nstd102humanPathogenic NCBI36 chr2: 233,599,457-242,717,007 , GRCh37.p13 chr2: 233,891,213-243,068,334 , GRCh38.p12 chr2: 233,026,503-242,126,183 UGT1A3, HDLBP, 194 more genes
    nsv3908885copy number variation1nstd102humanPathogenic NCBI36 chr2: 235,241,542-242,717,069 , GRCh38 chr2: 234,668,159-242,126,245 , GRCh37 chr2: 235,576,803-243,059,659 LOC105373946, TNRC17, 155 more genes
    nsv3908432copy number variation1nstd102humanPathogenic NCBI36 chr2: 237,540,145-242,656,032 , GRCh38 chr2: 236,966,763-242,065,208 , GRCh37 chr2: 237,875,406-243,007,359 COL6A3, LINC02610, 122 more genes
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