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Items: 1 to 20 of 103194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137796copy number variation1nstd102humanLikely benign GRCh37 chr9: 140,039,912-140,039,971 , GRCh38 chr9: 137,145,460-137,145,519 GRIN1
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137731copy number variation1nstd102humanBenign GRCh37 chrX: 1,412,907-1,412,990 , GRCh38 chrX: 1,294,014-1,294,097 , GRCh38 chrY: 1,294,014-1,294,097 , GRCh37 chrY: 1,362,907-1,362,990 CSF2RA, MIR3690
    nsv6137727copy number variation2nstd102humanUncertain significance GRCh38 chr3: 12,589,035-12,766,981 , GRCh37.p13 chr3: 12,630,534-12,808,480 RAF1, CRIP1P1, 1 more genes
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 TAOK2, SLC7A5P1, 44 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137686copy number variation1nstd102humanUncertain significance GRCh37 chr17: 29,687,722-29,704,696 , GRCh38.p12 chr17: 31,360,704-31,377,678 NF1
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6137663copy number variation1nstd102humannot provided GRCh38 chr2: 46,009,609-46,144,092 , GRCh37.p13 chr2: 46,236,748-46,371,231 PRKCE
    nsv6131680insertion1nstd186human GRCh37 chr16: 2,102,234-2,102,266 , GRCh38.p12 chr16: 2,052,233-2,052,265 TSC2
    nsv6131603insertion1nstd186human GRCh37 chr18: 60,565,268-60,565,299 , GRCh38.p12 chr18: 62,898,035-62,898,066 PHLPP1
    nsv6131472insertion1nstd186human GRCh37 chr18: 60,450,270-60,450,310 , GRCh38.p12 chr18: 62,783,037-62,783,077 PHLPP1
    nsv6131433insertion1nstd186human GRCh37 chr19: 7,131,019-7,131,019 , GRCh38.p12 chr19: 7,131,008-7,131,008 INSR
    nsv6131369insertion1nstd186human GRCh37 chr14: 102,316,011-102,316,011 , GRCh38.p12 chr14: 101,849,674-101,849,674 PPP2R5C
    nsv6131330insertion1nstd186human GRCh37 chr19: 46,892,658-46,892,677 , GRCh38.p12 chr19: 46,389,401-46,389,420 LOC105372426, PPP5C
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
    nsv6131079mobile element insertion1nstd186human GRCh37 chr17: 64,637,294-64,637,345 , GRCh38.p12 chr17: 66,641,176-66,641,227 PRKCA
    nsv6131008insertion1nstd186human GRCh37 chr17: 66,468,955-66,468,980 , GRCh38.p12 chr17: 68,472,814-68,472,839 PRKAR1A
    nsv6130857insertion1nstd186human GRCh37 chr22: 40,443,404-40,443,443 , GRCh38.p12 chr22: 40,047,400-40,047,439 TNRC6B
    nsv6130652insertion1nstd186human GRCh37 chr15: 79,285,608-79,285,608 , GRCh38.p12 chr15: 78,993,266-78,993,266 RASGRF1
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