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Items: 1 to 20 of 661

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7098835copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,344,058-89,061,168 , GRCh38.p12 chr4: 87,422,906-88,140,016 SPARCL1, DSPP, 13 more genes
    nsv7053656inversion1nstd229human GRCh38 chr4: 86,694,351-88,137,907 , GRCh37.p13 chr4: 87,615,504-89,059,059 KLHL8, GAPDHP60, 30 more genes
    nsv7050046inversion1nstd229human GRCh38 chr4: 85,500,769-88,545,032 , GRCh37.p13 chr4: 86,421,922-89,466,183 LOC105377326, NUDT9, 54 more genes
    nsv7049755inversion1nstd229human GRCh38 chr4: 88,218,307-88,227,402 , GRCh37.p13 chr4: 89,139,459-89,148,554 RNU6-1298P, ABCG2
    nsv6755702copy number variation1nstd229human GRCh38 chr4: 88,218,549-88,225,145 , GRCh37.p13 chr4: 89,139,701-89,146,297 RNU6-1298P, ABCG2
    nsv6752327copy number variation1nstd229human GRCh38 chr4: 88,105,357-91,750,216 , GRCh37.p13 chr4: 89,026,509-92,671,367 HERC5, SNCA, 34 more genes
    nsv6751924copy number variation1nstd229human GRCh38 chr4: 88,090,115-88,104,767 , GRCh37.p13 chr4: 89,011,267-89,025,919 ABCG2
    nsv6751806copy number variation1nstd229human GRCh38 chr4: 88,111,493-88,111,525 , GRCh37.p13 chr4: 89,032,645-89,032,677 ABCG2
    nsv6751530copy number variation1nstd229human GRCh38 chr4: 88,130,925-88,143,687 , GRCh37.p13 chr4: 89,052,077-89,064,839 ABCG2
    nsv6749121copy number variation1nstd229human GRCh38 chr4: 87,071,740-88,273,767 , GRCh37.p13 chr4: 87,992,892-89,194,919 RNU6-818P, DMP1, 29 more genes
    nsv6747638copy number variation1nstd229human GRCh38 chr4: 88,194,543-88,199,994 , GRCh37.p13 chr4: 89,115,695-89,121,146 ABCG2, RNU6-818P
    nsv6745301copy number variation1nstd229human GRCh38 chr4: 88,177,058-88,484,641 , GRCh37.p13 chr4: 89,098,210-89,405,792 RNU6-818P, HERC6, 9 more genes
    nsv6743506copy number variation1nstd229human GRCh38 chr4: 88,154,192-88,159,215 , GRCh37.p13 chr4: 89,075,344-89,080,367 ABCG2
    nsv6742927copy number variation1nstd229human GRCh38 chr4: 88,116,534-88,116,852 , GRCh37.p13 chr4: 89,037,686-89,038,004 ABCG2
    nsv6740695copy number variation1nstd229human GRCh38 chr4: 88,136,606-88,141,992 , GRCh37.p13 chr4: 89,057,758-89,063,144 ABCG2
    nsv6740013copy number variation1nstd229human GRCh38 chr4: 88,222,787-88,226,312 , GRCh37.p13 chr4: 89,143,939-89,147,464 ABCG2, RNU6-1298P
    nsv6739665copy number variation1nstd229human GRCh38 chr4: 88,110,401-88,117,300 , GRCh37.p13 chr4: 89,031,553-89,038,452 ABCG2
    nsv6738500copy number variation1nstd229human GRCh38 chr4: 88,023,767-88,203,759 , GRCh37.p13 chr4: 88,944,919-89,124,911 RPL31P24, ABCG2, 2 more genes
    nsv6574395inversion1nstd223human GRCh38 chr4: 87,923,661-89,968,732 , GRCh37.p13 chr4: 88,844,813-90,889,883 LOC102723458, LOC105377329, 33 more genes
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