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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044944inversion1nstd229human GRCh38 chr5: 83,059,964-83,060,186 , GRCh37.p13 chr5: 82,355,783-82,356,005 TMEM167A
    nsv6776346copy number variation1nstd229human GRCh38 chr5: 83,052,673-83,070,020 , GRCh37.p13 chr5: 82,348,492-82,365,839 SCARNA18, TMEM167A
    nsv6770571copy number variation1nstd229human GRCh38 chr5: 82,900,827-83,734,831 , GRCh37.p13 chr5: 82,196,646-83,030,650 LOC105379052, RN7SKP295, 14 more genes
    nsv6768013copy number variation1nstd229human GRCh38 chr5: 83,057,770-83,088,775 , GRCh37.p13 chr5: 82,353,589-82,384,594 SCARNA18, TMEM167A, 1 more genes
    nsv6764139copy number variation1nstd229human GRCh38 chr5: 83,075,360-83,077,198 , GRCh37.p13 chr5: 82,371,179-82,373,017 TMEM167A, XRCC4
    nsv6758602copy number variation1nstd229human GRCh38 chr5: 83,054,415-83,054,603 , GRCh37.p13 chr5: 82,350,234-82,350,422 TMEM167A
    nsv6573576inversion1nstd223human GRCh38 chr5: 83,060,557-83,061,414 , GRCh37.p13 chr5: 82,356,376-82,357,233 TMEM167A
    nsv6570069inversion1nstd223human GRCh38 chr5: 83,060,050-83,060,154 , GRCh37.p13 chr5: 82,355,869-82,355,973 TMEM167A
    nsv6408101copy number variation1nstd223human GRCh38 chr5: 83,063,886-83,064,502 , GRCh37.p13 chr5: 82,359,705-82,360,321 TMEM167A, SCARNA18
    nsv6407924copy number variation1nstd223human GRCh38 chr5: 83,069,786-83,070,510 , GRCh37.p13 chr5: 82,365,605-82,366,329 TMEM167A
    nsv6407483copy number variation1nstd223human GRCh38 chr5: 83,062,001-83,062,800 , GRCh37.p13 chr5: 82,357,820-82,358,619 SCARNA18, TMEM167A
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6135438copy number variation1nstd213human GRCh37 chr5: 80,920,000-86,370,001 , GRCh38.p12 chr5: 81,624,181-87,074,184 COX7C, HAPLN1, 56 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv6111975inversion1nstd212human GRCh38 chr5: 83,060,050-83,060,170 , GRCh37.p13 chr5: 82,355,869-82,355,989 TMEM167A
    nsv6067934insertion1nstd212human GRCh38 chr5: 83,060,042-83,060,042 , GRCh37.p13 chr5: 82,355,861-82,355,861 TMEM167A
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5729192mobile element insertion1nstd211human GRCh38 chr5: 83,060,167-83,060,167 , GRCh37.p13 chr5: 82,355,986-82,355,986 TMEM167A
    nsv5679814mobile element insertion2nstd211human GRCh38 chr5: 83,075,132-83,075,132 , GRCh37.p13 chr5: 82,370,951-82,370,951 TMEM167A
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