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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv6837613copy number variation1nstd229human GRCh38 chr7: 93,459,401-94,346,300 , GRCh37.p13 chr7: 93,088,713-93,975,612 TFPI2-DT, MIR489, 14 more genes
    nsv6833245copy number variation1nstd229human GRCh38 chr7: 93,811,346-93,985,533 , GRCh37.p13 chr7: 93,440,658-93,614,845 LOC105375402, GNG11, 5 more genes
    nsv6818581copy number variation1nstd229human GRCh38 chr7: 93,924,866-93,925,203 , GRCh37.p13 chr7: 93,554,178-93,554,515 LOC105375402, GNG11
    nsv6636808copy number variation1nstd102humanUncertain significance GRCh37 chr7: 93,325,684-93,594,362 , GRCh38.p12 chr7: 93,696,372-93,965,050 GNGT1, TFPI2, 6 more genes
    nsv6636693copy number variation1nstd102humanUncertain significance GRCh37 chr7: 93,539,781-93,623,201 , GRCh38.p12 chr7: 93,910,469-93,993,889 BET1, GNG11, 3 more genes
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 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
    nsv6602545copy number variation1nstd223human GRCh38 chr7: 93,811,345-93,985,532 , GRCh37.p13 chr7: 93,440,657-93,614,844 , GNG11, 6 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6137024copy number variation1nstd213human GRCh37 chr7: 93,400,000-97,690,001 , GRCh38.p12 chr7: 93,770,688-98,060,689 , SEM1, 77 more genes
    nsv6136214copy number variation1nstd213human GRCh37 chr7: 93,520,000-93,740,001 , GRCh38.p12 chr7: 93,890,688-94,110,689 , GNG11, 6 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv5683680mobile element insertion2nstd211human GRCh38 chr7: 93,928,130-93,928,130 , GRCh37.p13 chr7: 93,557,442-93,557,442 GNG11, LOC105375402
    nsv5641005insertion1nstd207human GRCh38 chr7: 93,928,116-93,928,116 , GRCh37.p13 chr7: 93,557,428-93,557,428 LOC105375402, GNG11
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5545390insertion1nstd206human GRCh38 chr7: 93,928,130-93,928,167 , GRCh37.p13 chr7: 93,557,442-93,557,479 LOC105375402, GNG11
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5119386mobile element insertion1nstd203human GRCh38 chr7: 93,928,116-93,928,130 , GRCh37.p13 chr7: 93,557,428-93,557,442 GNG11, LOC105375402
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