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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291226copy number variation1nstd102humanUncertain significance GRCh37 chr6: 80,298,478-80,372,195 , GRCh38.p12 chr6: 79,588,761-79,662,478 SH3BGRL2
    nsv3877550copy number variation1nstd102humanUncertain significance GRCh37 chr6: 80,298,478-80,362,940 , GRCh38.p12 chr6: 79,588,761-79,653,223 SH3BGRL2
    nsv4456630copy number variation1nstd102humanUncertain significance GRCh37 chr6: 80,238,027-80,487,813 , GRCh38.p12 chr6: 79,528,310-79,778,096 SH3BGRL2, LCA5
    nsv3884559copy number variation1nstd102humanUncertain significance GRCh37 chr6: 80,247,117-80,453,966 , GRCh38.p12 chr6: 79,537,400-79,744,249 SH3BGRL2, LCA5
    nsv6314264complex chromosomal rearrangement6nstd102humanPathogenic GRCh37 chr6: 8,071,078-8,071,078 , GRCh37 chr6: 78,901,159-78,901,159 , GRCh37 chr6: 80,345,233-80,345,233 , GRCh37 chr6: 8,070,204-8,070,204 , GRCh37 chr6: 80,345,233-80,345,233 , GRCh37 chr6: 81,020,656-81,020,656 , GRCh37 chr6: 78,901,159-78,901,159 , GRCh37 chr6: 81,021,339-81,021,339 , GRCh37 chr6: 82,288,681-82,288,681 , GRCh37 chr6: 82,288,681-82,288,681 , GRCh37 chr6: 86,681,515-86,681,515 , GRCh37 chr6: 86,681,515-86,681,515 , GRCh38.p12 chr6: 78,191,442-78,191,442 , GRCh38.p12 chr6: 81,578,964-81,578,964 , GRCh38.p12 chr6: 8,070,845-8,070,845 , GRCh38.p12 chr6: 78,191,442-78,191,442 , GRCh38.p12 chr6: 79,635,516-79,635,516 , GRCh38.p12 chr6: 80,310,939-80,310,939 , GRCh38.p12 chr6: 81,578,964-81,578,964 , GRCh38.p12 chr6: 85,971,797-85,971,797 , GRCh38.p12 chr6: 8,069,971-8,069,971 , GRCh38.p12 chr6: 79,635,516-79,635,516 , GRCh38.p12 chr6: 80,311,622-80,311,622 , GRCh38.p12 chr6: 85,971,797-85,971,797 SH3BGRL2, LOC105377865, 3 more genes
    nsv4682395copy number variation1nstd102humanUncertain significance GRCh37 chr6: 80,196,721-80,341,223 , GRCh38.p12 chr6: 79,487,004-79,631,506 SH3BGRL2, LOC100506851, 1 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 SH3BGRL2, LOC105377875, 188 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SH3BGRL2, SPACA1, 187 more genes
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 SH3BGRL2, MRAP2, 125 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 SH3BGRL2, RPS27P15, 118 more genes
    nsv7097093copy number variation2nstd102humanPathogenic GRCh37 chr6: 79,650,410-80,912,949 , GRCh38.p12 chr6: 78,940,693-80,203,232 SH3BGRL2, LOC107986614, 22 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 SH3BGRL2, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 SH3BGRL2, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SH3BGRL2, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 SH3BGRL2, ITPR3, 2905 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 SH3BGRL2, RNU6-770P, 810 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 SH3BGRL2, HLA-DPB2, 1001 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 SH3BGRL2, LOC101928570, 288 more genes
    nsv3911622copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 79,678,455-84,862,865 , GRCh37.p13 chr6: 79,621,736-84,806,146 , GRCh38.p12 chr6: 78,912,019-84,096,427 SH3BGRL2, BCKDHB, 55 more genes
    nsv4674953copy number variation1nstd102humanLikely benign GRCh37 chr6: 80,113,392-80,351,699 , GRCh38.p12 chr6: 79,403,675-79,641,982 SH3BGRL2, LCA5, 4 more genes
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