prss35[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3880998	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 83,788,069-84,228,464 , GRCh38.p12 chr6: 83,078,350-83,518,745	PRSS35, PGM3, 3 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	PRSS35, SPACA1, 187 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	PRSS35, ME1, 136 more genes
nsv3889959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055	PRSS35, MRAP2, 125 more genes
nsv3873582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,319,012-91,907,669 , GRCh38.p12 chr6: 82,609,295-91,197,951	PRSS35, LOC105377882, 117 more genes
nsv6290989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748	PRSS35, KRT18P30, 58 more genes
nsv7098884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093	PRSS35, LOC105377879, 47 more genes
nsv1398415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,013,454-84,395,825 , GRCh38.p12 chr6: 82,303,737-83,686,106	PRSS35, PGM3, 10 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	PRSS35, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	PRSS35, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	PRSS35, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	PRSS35, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	PRSS35, RNU6-770P, 810 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	PRSS35, LOC101928570, 288 more genes
nsv3872975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393	PRSS35, ME1, 178 more genes
nsv3911622	copy number variation	1	nstd102	human	Likely 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	PRSS35, BCKDHB, 55 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	PRSS35, MTHFD2P2, 212 more genes
nsv5381391	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 83,878,953-84,567,108 , GRCh38.p12 chr6: 83,169,234-83,857,389	PRSS35, DOP1A, 6 more genes

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