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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097093copy number variation2nstd102humanPathogenic GRCh37 chr6: 79,650,410-80,912,949 , GRCh38.p12 chr6: 78,940,693-80,203,232 LOC107986614, LOC643562, 22 more genes
    nsv7054859inversion1nstd229human GRCh38 chr6: 78,924,246-79,955,220 , GRCh37.p13 chr6: 79,633,963-80,664,937 PHIP, HMGN3, 17 more genes
    nsv6793081copy number variation1nstd229human GRCh38 chr6: 79,287,673-79,316,084 , GRCh37.p13 chr6: 79,997,390-80,025,801 LCAL1
    nsv6791355copy number variation1nstd229human GRCh38 chr6: 78,644,070-79,657,413 , GRCh37.p13 chr6: 79,353,787-80,367,130 HMGN3-AS1, LOC105377867, 13 more genes
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6636747copy number variation1nstd102humanUncertain significance GRCh37 chr6: 77,773,778-80,880,138 , GRCh38.p12 chr6: 77,064,061-80,170,421 TRF-GAA8-1, HMGN3-AS1, 31 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 RPS27P15, COX7A2, 118 more genes
    nsv4729340copy number variation1nstd102humanPathogenic GRCh37 chr6: 74,226,559-80,208,037 , GRCh38.p12 chr6: 73,516,836-79,498,320 LOC107986613, LOC101928516, 58 more genes
    nsv4675505copy number variation1nstd102humanLikely benign GRCh37 chr6: 79,999,914-80,315,818 , GRCh38.p12 chr6: 79,290,197-79,606,101 LCA5, LOC100506851, 5 more genes
    nsv4456122copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,216,253-82,753,743 , GRCh38.p12 chr6: 77,506,536-82,044,026 LOC105377869, AK4P5, 38 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4145803copy number variation1nstd166human GRCh37.p13 chr6: 80,000,546-80,316,177 , GRCh38.p12 chr6: 79,290,829-79,606,460 , DBIP1, 6 more genes
    nsv4134335copy number variation1nstd166human GRCh37.p13 chr6: 79,964,808-80,076,437 , GRCh38.p12 chr6: 79,255,091-79,366,720 LCAL1, LOC112267976
    nsv3924632copy number variation1nstd102humanUncertain significance GRCh38 chr6: 78,661,176-80,245,532 , NCBI36 chr6: 79,427,612-81,011,968 , GRCh37 chr6: 79,370,893-80,955,249 LOC107986613, LCA5, 23 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 LOC105377875, KCNQ5-IT1, 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 SPACA1, TAF13P1, 187 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 RNU6-770P, MAP3K5-AS2, 810 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 BCKDHB, DBIP1, 55 more genes
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