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Items: 1 to 20 of 303

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    nsv5463676copy number variation1nstd206human GRCh38 chr7: 1,527,650-1,529,428 , GRCh37.p13 chr7: 1,567,286-1,569,064 MAFK
    nsv5463122copy number variation1nstd206human GRCh38 chr7: 1,540,393-1,541,790 , GRCh37.p13 chr7: 1,580,029-1,581,426 MAFK, TMEM184A
    nsv4953209copy number variation1nstd200human GRCh38 chr7: 1,441,829-1,562,070 , GRCh37.p13 chr7: 1,481,465-1,601,706 MAFK, MICALL2, 4 more genes
    nsv4949540copy number variation1nstd200human GRCh38 chr7: 1,537,989-1,549,884 , GRCh37.p13 chr7: 1,577,625-1,589,520 TMEM184A, MAFK
    nsv4729632copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,063,598-1,614,261 , GRCh38.p12 chr7: 1,023,962-1,574,625 MICALL2, INTS1, 14 more genes
    nsv4729496copy number variation1nstd102humanUncertain significance GRCh37 chr7: 967,185-1,781,553 , GRCh38.p12 chr7: 927,549-1,741,917 ZFAND2A, LOC105375124, 25 more genes
    nsv4707113copy number variation1nstd195human GRCh37 chr7: 1,486,301-1,657,751 , GRCh38.p12 chr7: 1,446,665-1,618,115 , LOC100128653, 10 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 C7orf50, LOC105375123, 47 more genes
    nsv4675619copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,108,122-1,812,800 , GRCh38.p12 chr7: 1,068,486-1,773,164 ELFN1, PSMG3, 20 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 LOC112267991, MICALL2, 42 more genes
    nsv4675062copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,065,860-1,812,800 , GRCh38.p12 chr7: 1,026,224-1,773,164 INTS1, MICALL2, 21 more genes
    nsv4612781copy number variation1nstd183human GRCh37 chr7: 1,423,055-1,575,377 , GRCh38.p12 chr7: 1,383,419-1,535,741 INTS1, LOC100128653, 3 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 LOC442497, LFNG, 85 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4393209copy number variation1nstd174human GRCh37 chr7: 1,420,901-1,715,300 , GRCh38.p12 chr7: 1,381,265-1,675,664 , PSMG3-AS1, 12 more genes
    nsv3924735copy number variation1nstd102humanUncertain significance NCBI36 chr7: 1,337,149-2,536,804 , GRCh38 chr7: 1,330,987-2,530,644 , GRCh37 chr7: 1,370,623-2,570,278 TFAMP1, CHST12, 32 more genes
    nsv3923348copy number variation1nstd102humanPathogenic NCBI36 chr7: 149,268-6,644,183 , GRCh37 chr7: 54,185-6,677,658 , GRCh38 chr7: 54,185-6,638,027 ZNF890P, FOXK1, 143 more genes
    nsv3922360copy number variation1nstd102humanUncertain significance GRCh37 chr7: 729,191-2,071,156 , GRCh38 chr7: 689,554-2,031,521 , NCBI36 chr7: 695,717-2,037,682 LOC102723758, GET4, 32 more genes
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