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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6858001copy number variation1nstd229human GRCh38 chr8: 81,411,201-81,548,500 , GRCh37.p13 chr8: 82,323,436-82,460,735 PMP2, FABP12, 4 more genes
    nsv6857070copy number variation1nstd229human GRCh38 chr8: 81,400,181-81,495,843 , GRCh37.p13 chr8: 82,312,416-82,408,078 FABP9, FABP4, 2 more genes
    nsv6852616copy number variation1nstd229human GRCh38 chr8: 81,434,776-81,463,115 , GRCh37.p13 chr8: 82,347,011-82,375,350 FABP9, PMP2, 1 more genes
    nsv6850513copy number variation1nstd229human GRCh38 chr8: 81,454,355-81,462,197 , GRCh37.p13 chr8: 82,366,590-82,374,432 LOC101927118, FABP9
    nsv6850477copy number variation1nstd229human GRCh38 chr8: 81,438,321-81,467,240 , GRCh37.p13 chr8: 82,350,556-82,379,475 FABP9, PMP2, 1 more genes
    nsv6636819copy number variation1nstd102humanUncertain significance GRCh37 chr8: 79,876,744-83,112,711 , GRCh38.p12 chr8: 78,964,509-82,200,476 SLC25A51P3, PMP2, 59 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6432269copy number variation1nstd223human GRCh38 chr8: 80,979,001-81,477,900 , GRCh37.p13 chr8: 81,891,236-82,390,135 LOC105375924, PMP2, 8 more genes
    nsv6423458copy number variation1nstd223human GRCh38 chr8: 81,460,174-81,461,158 , GRCh37.p13 chr8: 82,372,409-82,373,393 FABP9, LOC101927118
    nsv6315163copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854 ZNF704, RN7SL107P, 137 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313579copy number variation1nstd102humanPathogenic GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479 LOC105375915, LOC105375918, 143 more genes
    nsv6313526copy number variation1nstd102humanUncertain significance GRCh37 chr8: 82,353,502-82,673,333 , GRCh38.p12 chr8: 81,441,267-81,761,098 PMP2, IMPA1, 12 more genes
    nsv6291603copy number variation1nstd102humanUncertain significance GRCh38 chr8: 81,061,071-81,682,394 , GRCh37.p13 chr8: 81,973,306-82,594,629 FABP9, LOC105375926, 15 more genes
    nsv6291447copy number variation1nstd102humanUncertain significance GRCh37 chr8: 81,991,684-82,523,573 , GRCh38.p12 chr8: 81,079,449-81,611,338 LOC105375924, IMPA1P1, 11 more genes
    nsv6290934copy number variation1nstd102humanUncertain significance GRCh37 chr8: 81,829,690-85,173,253 , GRCh38.p12 chr8: 80,917,455-84,261,018 RALYL, SNX16, 33 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136596copy number variation1nstd213human GRCh37 chr8: 72,190,000-86,530,001 , GRCh38.p12 chr8: 71,277,765-85,617,772 ACTBP6, CA2, 173 more genes
    nsv6136078copy number variation1nstd213human GRCh37 chr8: 81,690,000-83,510,001 , GRCh38.p12 chr8: 80,777,765-82,597,766 FABP4, FABP9, 27 more genes
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