878296 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv428159	copy number variation	7	nstd8	human		NCBI36 chr7: 42,475-311,691 , GRCh37.p13 chr7: 10,239-216,608 , GRCh38.p12 chr7: 43,902-216,608 , GRCh38.p12 chr7\|NT_187558.1: 1-157,952 , GRCh38.p12 chr7\|NT_187653.1: 36,223-190,869	FAM20C, LINC03014, 6 more genes

Supplemental Content

nssv450913 (1)
dbVar
excitatory amino acid transporter 1 isoform X1 [Homo sapiens]
excitatory amino acid transporter 1 isoform X1 [Homo sapiens]
gi|530378898|ref|XP_005248399.1|

Protein
PREDICTED: Homo sapiens solute carrier family 1 member 3 (SLC1A3), transcript va...
PREDICTED: Homo sapiens solute carrier family 1 member 3 (SLC1A3), transcript variant X3, mRNA
gi|2462603774|ref|XM_054353191.1|

Nucleotide
Homo sapiens solute carrier family 1 member 3 (SLC1A3), RefSeqGene on chromosome...
Homo sapiens solute carrier family 1 member 3 (SLC1A3), RefSeqGene on chromosome 5
gi|269308196|ref|NG_015890.1|

Nucleotide

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dbVar