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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6824081copy number variation1nstd229human GRCh38 chr7: 44,868,531-44,876,039 , GRCh37.p13 chr7: 44,908,130-44,915,638 PURB
    nsv6821522copy number variation1nstd229human GRCh38 chr7: 44,637,314-45,095,725 , GRCh37.p13 chr7: 44,676,913-45,135,324 PURB, MYO1G, 14 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
    nsv6613872copy number variation1nstd223human GRCh38 chr7: 44,883,901-44,886,000 , GRCh37.p13 chr7: 44,923,500-44,925,599 PURB
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313816copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,765,589-45,364,793 , GRCh38.p12 chr7: 44,725,990-45,325,194 LOC100419775, H2AZ2-DT, 20 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135995copy number variation1nstd213human GRCh37 chr7: 44,480,000-45,360,001 , GRCh38.p12 chr7: 44,440,401-45,320,402 PURB, NPC1L1, 28 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 more genes
    nsv6135768copy number variation1nstd213human GRCh37 chr7: 44,920,000-45,020,001 , GRCh38.p12 chr7: 44,880,401-44,980,402 PURB, MYO1G, 3 more genes
    nsv6075719insertion1nstd212human GRCh38 chr7: 44,875,999-44,875,999 , GRCh37.p13 chr7: 44,915,598-44,915,598 PURB
    nsv6073577insertion1nstd212human GRCh38 chr7: 44,883,774-44,883,774 , GRCh37.p13 chr7: 44,923,373-44,923,373 PURB
    nsv6066831insertion1nstd212human GRCh38 chr7: 44,883,803-44,883,803 , GRCh37.p13 chr7: 44,923,402-44,923,402 PURB
    nsv5678341mobile element insertion1nstd211human GRCh38 chr7: 44,876,005-44,876,005 , GRCh37.p13 chr7: 44,915,604-44,915,604 PURB
    nsv5636883insertion1nstd207human GRCh38 chr7: 44,883,774-44,883,774 , GRCh37.p13 chr7: 44,923,373-44,923,373 PURB
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493220copy number variation1nstd206human GRCh38 chr7: 44,883,774-44,883,827 , GRCh37.p13 chr7: 44,923,373-44,923,426 PURB
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