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Items: 1 to 20 of 77498

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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
    nsv6131680insertion1nstd186human GRCh37 chr16: 2,102,234-2,102,266 , GRCh38.p12 chr16: 2,052,233-2,052,265 TSC2
    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
    nsv6130780insertion1nstd186human GRCh37 chr13: 50,015,380-50,015,415 , GRCh38.p12 chr13: 49,441,244-49,441,279 CAB39L
    nsv6130652insertion1nstd186human GRCh37 chr15: 79,285,608-79,285,608 , GRCh38.p12 chr15: 78,993,266-78,993,266 RASGRF1
    nsv6130356insertion1nstd186human GRCh37 chr19: 40,734,606-40,734,638 , GRCh38.p12 chr19: 40,228,699-40,228,731 AKT2
    nsv6130283insertion1nstd186human GRCh37 chr13: 114,749,839-114,749,879 , GRCh38.p12 chr13: 113,980,428-113,980,468 , GRCh38.p12 chr13|NW_011332698.1: 43,454-43,494 RASA3
    nsv6130243insertion1nstd186human GRCh37 chr12: 102,799,045-102,799,080 , GRCh38.p12 chr12: 102,405,267-102,405,302 IGF1, LINC02456
    nsv6129965mobile element insertion1nstd186human GRCh37 chr12: 118,186,938-118,186,989 , GRCh38.p12 chr12: 117,749,133-117,749,184 KSR2
    nsv6129865insertion1nstd186human GRCh37 chr15: 38,801,306-38,801,336 , GRCh38.p12 chr15: 38,509,105-38,509,135 RASGRP1, LOC105370774
    nsv6129737insertion1nstd186human GRCh37 chr16: 10,153,199-10,153,245 , GRCh38.p12 chr16: 10,059,342-10,059,388 GRIN2A
    nsv6129599insertion1nstd186human GRCh37 chr19: 643,120-643,155 , GRCh38.p12 chr19: 643,120-643,155 FGF22
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