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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046126inversion1nstd229human GRCh38 chr6: 81,393,479-82,767,602 , GRCh37.p13 chr6: 82,103,196-83,477,319 LOC107986617, IBTK, 12 more genes
    nsv7039272inversion1nstd229human GRCh38 chr6: 81,812,964-81,813,029 , GRCh37.p13 chr6: 82,522,681-82,522,746 LINC01526
    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
    nsv6783925copy number variation1nstd229human GRCh38 chr6: 81,691,926-82,286,650 , GRCh37.p13 chr6: 82,401,643-82,996,367 RNU6-130P, LOC105377874, 7 more genes
    nsv6779356copy number variation1nstd229human GRCh38 chr6: 80,800,138-81,949,180 , GRCh37.p13 chr6: 81,509,855-82,658,897 LOC105377873, LINC02542, 4 more genes
    nsv6636874copy number variation1nstd102humanUncertain significance GRCh37 chr6: 81,087,736-84,200,632 , GRCh38.p12 chr6: 80,378,019-83,490,913 PGM3, ME1, 24 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
    nsv4945350copy number variation1nstd200human GRCh38 chr6: 81,691,926-82,286,650 , GRCh37.p13 chr6: 82,401,643-82,996,367 , LINC01526, 8 more genes
    nsv4566083mobile element insertion1nstd166human GRCh37.p13 chr6: 82,523,356-82,523,356 , GRCh38.p12 chr6: 81,813,639-81,813,639 LINC01526
    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
    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
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 MRAP2, LCA5, 125 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
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