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Items: 1 to 20 of 28

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312507copy number variation1nstd102humanPathogenic GRCh37 chr6: 75,855,798-75,861,023 , GRCh38.p12 chr6: 75,146,082-75,151,307 COL12A1
    nsv6312547copy number variation1nstd102humanPathogenic GRCh37 chr6: 75,833,723-75,833,798 , GRCh38 chr6: 75,124,007-75,124,082 COL12A1
    nsv7093454delins1nstd102humanLikely pathogenic GRCh38 chr6: 75,102,633-75,102,707 , GRCh37 chr6: 75,812,349-75,812,423 COL12A1
    nsv6312409copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,806,949-75,807,042 , GRCh38.p12 chr6: 75,097,233-75,097,326 COL12A1
    nsv7097590copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,858,054-75,912,508 , GRCh38.p12 chr6: 75,148,338-75,202,792 COL12A1
    nsv6312066copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,796,263-75,813,546 , GRCh38.p12 chr6: 75,086,547-75,103,830 COL12A1
    nsv7093461delins1nstd102humanUncertain significance GRCh38 chr6: 75,181,157-75,181,158 , GRCh37 chr6: 75,890,873-75,890,874 COL12A1
    nsv6312067copy number variation1nstd102humanPathogenic GRCh37 chr6: 75,833,026-75,912,508 , GRCh38.p12 chr6: 75,123,310-75,202,792 COL12A1, SNORD156
    nsv4681877copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr6: 75,796,253-75,912,518 , GRCh38.p12 chr6: 75,086,537-75,202,802 COL12A1, SNORD156
    nsv5381533copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,796,253-75,855,181 , GRCh38.p12 chr6: 75,086,537-75,145,465 COL12A1, SNORD156
    nsv7097848copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,833,644-75,847,315 , GRCh38.p12 chr6: 75,123,928-75,137,599 COL12A1, SNORD156
    nsv3871830copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,184,521-75,899,477 , GRCh38.p12 chr6: 74,474,805-75,189,761 COL12A1, LOC101928516, 3 more genes
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 COL12A1, LOC105377875, 188 more genes
    nsv6315402copy number variation1nstd102humanPathogenic GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961 COL12A1, LOC105377841, 139 more genes
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 COL12A1, MRAP2, 125 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 COL12A1, RPS27P15, 118 more genes
    nsv6291339copy number variation1nstd102humanPathogenic GRCh37 chr6: 70,165,296-79,920,769 , GRCh38.p12 chr6: 69,455,404-79,211,052 COL12A1, RNU6-84P, 113 more genes
    nsv4729340copy number variation1nstd102humanPathogenic GRCh37 chr6: 74,226,559-80,208,037 , GRCh38.p12 chr6: 73,516,836-79,498,320 COL12A1, LOC107986613, 58 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 COL12A1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 COL12A1, RNU6-411P, 2910 more genes
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