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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6816366copy number variation1nstd229human GRCh38 chr7: 1,503,442-1,561,054 , GRCh37.p13 chr7: 1,543,078-1,600,690 TMEM184A, INTS1, 2 more genes
    nsv6808805copy number variation1nstd229human GRCh38 chr7: 1,531,587-1,537,754 , GRCh37.p13 chr7: 1,571,223-1,577,390 MAFK, LOC100128653
    nsv6636500copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,316,239-1,781,553 , GRCh38.p12 chr7: 1,276,603-1,741,917 LOC105375124, ELFN1, 13 more genes
    nsv6635470copy number variation1nstd227human GRCh37 chr7: 1,563,025-1,596,196 , GRCh38.p12 chr7: 1,523,389-1,556,560 MAFK, TMEM184A, 1 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632476copy number variation1nstd224human GRCh37 chr7: 93,811-2,255,893 , GRCh38.p12 chr7: 93,811-2,216,258 INTS1, DNAAF5, 52 more genes
    nsv6602617copy number variation1nstd223human GRCh38 chr7: 1,530,411-1,530,626 , GRCh37.p13 chr7: 1,570,047-1,570,262 MAFK, LOC100128653
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6290977copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,330,065-1,821,278 , GRCh38.p12 chr7: 1,290,429-1,781,642 LOC105375303, PSMG3, 13 more genes
    nsv6290909copy number variation1nstd102humanUncertain significance GRCh37 chr7: 989,697-2,138,529 , GRCh38.p12 chr7: 950,061-2,098,894 PSMG3, TFAMP1, 29 more genes
    nsv6136189copy number variation1nstd213human GRCh37 chr7: 520,000-1,870,001 , GRCh38.p12 chr7: 480,363-1,830,365 MAD1L1, SUN1, 35 more genes
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    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
    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
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