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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5449548copy number variation1nstd206human GRCh38 chr2: 306,000-862,000 , GRCh37.p13 chr2: 306,000-857,686 , LOC105373480, 12 more genes
    nsv4904659copy number variation1nstd200human GRCh38 chr2: 197,015-655,136 , GRCh37.p13 chr2: 197,015-655,136 ACP1, SH3YL1, 9 more genes
    nsv4904657copy number variation1nstd200human GRCh38 chr2: 132,469-641,802 , GRCh37.p13 chr2: 132,469-641,802 SH3YL1, LOC105373324, 10 more genes
    nsv4788196copy number variation1nstd200human GRCh37 chr2: 373,988-945,132 , GRCh38.p12 chr2: 373,988-949,446 , LINC01874, 14 more genes
    nsv4728591copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-1,126,253 , GRCh38.p12 chr2: 12,770-1,130,567 LOC105373351, LINC01875, 20 more genes
    nsv4728162copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-1,680,334 , GRCh38.p12 chr2: 12,770-1,676,562 LINC01874, LOC105373346, 24 more genes
    nsv4715102copy number variation1nstd195human GRCh37 chr2: 556,301-671,251 , GRCh38.p12 chr2: 556,301-671,251 TMEM18, LOC105373352
    nsv4706713copy number variation1nstd195human GRCh37 chr2: 488,601-556,251 , GRCh38.p12 chr2: 488,601-556,251 LINC01874, LOC100996637, 2 more genes
    nsv4679749copy number variation1nstd189human GRCh37.p13 chr2: 445,186-944,427 , GRCh38.p12 chr2: 445,186-948,741 , TMEM18, 12 more genes
    nsv4674039copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-3,000,954 , GRCh38.p12 chr2: 12,770-2,997,182 LINC01115, LOC105373352, 31 more genes
    nsv4585876copy number variation1nstd183human GRCh37 chr2: 391,921-577,246 , GRCh38.p12 chr2: 391,921-577,246 LINC01874, LOC100996637, 2 more genes
    nsv4583893copy number variation1nstd183human GRCh37 chr2: 382,409-737,505 , GRCh38.p12 chr2: 382,409-737,505 TMEM18-DT, LINC01875, 8 more genes
    nsv4454966copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665 LINC01810, ADI1, 83 more genes
    nsv4453225copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-2,832,894 , GRCh38.p12 chr2: 12,770-2,829,122 LOC105373359, LOC107985839, 29 more genes
    nsv4452632copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-3,819,558 , GRCh38.p12 chr2: 12,770-3,771,968 LOC107985838, LOC100996637, 45 more genes
    nsv4449985copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-2,348,876 , GRCh38.p12 chr2: 12,770-2,345,104 PXDN, TPO, 27 more genes
    nsv4404477copy number variation1nstd174human GRCh37 chr2: 559,913-1,428,202 , GRCh38.p12 chr2: 559,913-1,424,430 , SNTG2, 12 more genes
    nsv4395739copy number variation1nstd174human GRCh37 chr2: 314,425-856,963 , GRCh38.p12 chr2: 314,425-861,277 , LINC01115, 12 more genes
    nsv4381038copy number variation1nstd173human GRCh37 chr2: 319,721-857,286 , GRCh38.p12 chr2: 319,721-861,600 , TMEM18-DT, 11 more genes
    nsv4068442copy number variation1nstd166human GRCh37.p13 chr2: 197,016-655,135 , GRCh38.p12 chr2: 197,016-655,135 SH3YL1, LINC01865, 9 more genes
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