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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6137718copy number variation1nstd102humanBenign GRCh38 chr12: 20,679,864-20,679,919 , GRCh37 chr12: 20,832,798-20,832,853 PDE3A, SLCO1C1
    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
    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
    nsv6131704insertion1nstd186human GRCh37 chr18: 77,224,671-77,224,680 , GRCh38.p12 chr18: 79,464,671-79,464,680 NFATC1, LOC101927897
    nsv6131433insertion1nstd186human GRCh37 chr19: 7,131,019-7,131,019 , GRCh38.p12 chr19: 7,131,008-7,131,008 INSR
    nsv6131413insertion1nstd186human GRCh37 chr19: 46,022,710-46,023,020 , GRCh38.p12 chr19: 45,519,452-45,519,762 VASP, LOC107985315
    nsv6131193insertion1nstd186human GRCh37 chr18: 77,160,842-77,160,883 , GRCh38.p12 chr18: 79,400,842-79,400,883 NFATC1
    nsv6131062insertion1nstd186human GRCh37 chr19: 47,954,579-47,954,617 , GRCh38.p12 chr19: 47,451,322-47,451,360 SLC8A2
    nsv6130735insertion1nstd186human GRCh37 chr16: 68,126,512-68,126,512 , GRCh38.p12 chr16: 68,092,609-68,092,609 NFATC3
    nsv6130729mobile element insertion1nstd186human GRCh37 chr5: 159,351,199-159,351,250 , GRCh38.p12 chr5: 159,924,192-159,924,243 ADRA1B
    nsv6130356insertion1nstd186human GRCh37 chr19: 40,734,606-40,734,638 , GRCh38.p12 chr19: 40,228,699-40,228,731 AKT2
    nsv6130204insertion1nstd186human GRCh37 chr18: 77,241,814-77,241,832 , GRCh38.p12 chr18: 79,481,814-79,481,832 NFATC1
    nsv6130114insertion1nstd186human GRCh37 chr18: 77,227,360-77,227,385 , GRCh38.p12 chr18: 79,467,360-79,467,385 NFATC1, LOC101927897, 1 more genes
    nsv6130058insertion1nstd186human GRCh37 chr19: 7,153,378-7,153,378 , GRCh38.p12 chr19: 7,153,367-7,153,367 INSR
    nsv6129462insertion1nstd186human GRCh37 chr14: 24,794,428-24,794,428 , GRCh38.p12 chr14: 24,325,222-24,325,222 , GRCh38.p12 chr14|NW_018654722.1: 626,200-626,200 ADCY4
    nsv6129266insertion1nstd186human GRCh37 chr20: 50,024,987-50,024,987 , GRCh38.p12 chr20: 51,408,450-51,408,450 NFATC2
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