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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147771insertion1nstd232human GRCh37.p13 chr6: 90,049,360-90,049,360 , GRCh38.p12 chr6: 89,339,641-89,339,641 UBE2J1
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6810917copy number variation1nstd229human GRCh38 chr6: 89,351,503-89,515,933 , GRCh37.p13 chr6: 90,061,222-90,225,652 ANKRD6, UBE2J1, 4 more genes
    nsv6810708copy number variation1nstd229human GRCh38 chr6: 89,314,111-89,598,350 , GRCh37.p13 chr6: 90,023,830-90,308,069 RN7SL11P, LOC105377889, 5 more genes
    nsv6808401copy number variation1nstd229human GRCh38 chr6: 89,111,826-89,628,748 , GRCh37.p13 chr6: 89,821,545-90,338,467 GABRR1, TUBB3P1, 10 more genes
    nsv6807733copy number variation1nstd229human GRCh38 chr6: 89,290,655-89,430,422 , GRCh37.p13 chr6: 90,000,374-90,140,141 TUBB3P1, UBE2J1, 3 more genes
    nsv6802932copy number variation1nstd229human GRCh38 chr6: 88,525,377-89,929,877 , GRCh37.p13 chr6: 89,235,096-90,639,596 GJA10, RN7SL11P, 27 more genes
    nsv6800503copy number variation1nstd229human GRCh38 chr6: 89,009,911-89,699,384 , GRCh37.p13 chr6: 89,719,630-90,409,103 RRAGD, MDN1-AS1, 17 more genes
    nsv6798646copy number variation1nstd229human GRCh38 chr6: 89,341,498-89,735,839 , GRCh37.p13 chr6: 90,051,217-90,445,558 NACAP7, MDN1-AS1, 7 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6413108copy number variation1nstd223human GRCh38 chr6: 89,111,826-89,628,748 , GRCh37.p13 chr6: 89,821,545-90,338,467 RN7SL11P, LOC105377889, 10 more genes
    nsv6400895copy number variation1nstd223human GRCh38 chr6: 89,338,965-89,341,026 , GRCh37.p13 chr6: 90,048,684-90,050,745 UBE2J1
    nsv6397345copy number variation1nstd223human GRCh38 chr6: 89,336,894-89,338,145 , GRCh37.p13 chr6: 90,046,613-90,047,864 UBE2J1
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6290854copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,008,961-93,761,490 , GRCh38.p12 chr6: 89,299,242-93,051,772 NACAP7, PIMREGP3, 38 more genes
    nsv6135855copy number variation1nstd213human GRCh37 chr6: 87,530,000-91,880,001 , GRCh38.p12 chr6: 86,820,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv6135528copy number variation1nstd213human GRCh37 chr6: 89,680,000-90,050,001 , GRCh38.p12 chr6: 88,970,281-89,340,282 GABRR1, GABRR2, 10 more genes
    nsv6135527copy number variation1nstd213human GRCh37 chr6: 87,520,000-91,880,001 , GRCh38.p12 chr6: 86,810,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv6079590insertion1nstd212human GRCh38 chr6: 89,339,647-89,339,647 , GRCh37.p13 chr6: 90,049,366-90,049,366 UBE2J1
    nsv6067857insertion1nstd212human GRCh38 chr6: 89,339,545-89,339,545 , GRCh37.p13 chr6: 90,049,264-90,049,264 UBE2J1
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